These samples need more evidence before they can be counted. This includes samples without a confirmed case/control role.
primary colorectal cancer AMC_2-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228184
sample_title: primary colorectal cancer AMC_2-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_3-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228185
sample_title: primary colorectal cancer AMC_3-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_5-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228186
sample_title: primary colorectal cancer AMC_5-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_6-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228187
sample_title: primary colorectal cancer AMC_6-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_7-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228188
sample_title: primary colorectal cancer AMC_7-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_8-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228189
sample_title: primary colorectal cancer AMC_8-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_9-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228190
sample_title: primary colorectal cancer AMC_9-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_10-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228191
sample_title: primary colorectal cancer AMC_10-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_12-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228192
sample_title: primary colorectal cancer AMC_12-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_13-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228193
sample_title: primary colorectal cancer AMC_13-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_17-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228194
sample_title: primary colorectal cancer AMC_17-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_18-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228195
sample_title: primary colorectal cancer AMC_18-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_19-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228196
sample_title: primary colorectal cancer AMC_19-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_20-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228197
sample_title: primary colorectal cancer AMC_20-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_21-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228198
sample_title: primary colorectal cancer AMC_21-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_22-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228199
sample_title: primary colorectal cancer AMC_22-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_23-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228200
sample_title: primary colorectal cancer AMC_23-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
primary colorectal cancer AMC_24-1
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- primary colorectal cancer
- Characteristics
- tissue: primary colorectal cancer; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228201
sample_title: primary colorectal cancer AMC_24-1
source_name: primary colorectal cancer
characteristics: tissue: primary colorectal cancer; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_2-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228202
sample_title: normal colon AMC_2-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_3-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228203
sample_title: normal colon AMC_3-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_5-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228204
sample_title: normal colon AMC_5-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_6-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228205
sample_title: normal colon AMC_6-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_7-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228206
sample_title: normal colon AMC_7-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_8-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228207
sample_title: normal colon AMC_8-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_9-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228208
sample_title: normal colon AMC_9-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_10-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228209
sample_title: normal colon AMC_10-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_12-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228210
sample_title: normal colon AMC_12-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_13-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228211
sample_title: normal colon AMC_13-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_17-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228212
sample_title: normal colon AMC_17-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_18-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228213
sample_title: normal colon AMC_18-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_19-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228214
sample_title: normal colon AMC_19-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_20-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228215
sample_title: normal colon AMC_20-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_21-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228216
sample_title: normal colon AMC_21-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_22-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228217
sample_title: normal colon AMC_22-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_23-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228218
sample_title: normal colon AMC_23-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
normal colon AMC_24-2
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Sample-local control marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- normal colon
- Characteristics
- tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228219
sample_title: normal colon AMC_24-2
source_name: normal colon
characteristics: tissue: normal-looking surrounding colonic epithelium; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_2-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228220
sample_title: metastasized cancer AMC_2-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_3-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228221
sample_title: metastasized cancer AMC_3-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_5-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228222
sample_title: metastasized cancer AMC_5-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_6-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228223
sample_title: metastasized cancer AMC_6-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_7-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228224
sample_title: metastasized cancer AMC_7-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_8-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228225
sample_title: metastasized cancer AMC_8-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_9-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228226
sample_title: metastasized cancer AMC_9-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_10-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228227
sample_title: metastasized cancer AMC_10-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_12-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228228
sample_title: metastasized cancer AMC_12-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_13-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228229
sample_title: metastasized cancer AMC_13-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_17-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228230
sample_title: metastasized cancer AMC_17-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_18-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228231
sample_title: metastasized cancer AMC_18-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_19-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228232
sample_title: metastasized cancer AMC_19-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_20-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228233
sample_title: metastasized cancer AMC_20-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_21-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228234
sample_title: metastasized cancer AMC_21-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_22-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228235
sample_title: metastasized cancer AMC_22-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_23-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228236
sample_title: metastasized cancer AMC_23-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq
metastasized cancer AMC_24-3
Not included: the study role or selected requirements have incomplete or conflicting evidence. specimen category: Tissue or biopsy — Insufficient evidence. Study role: Case marker detected.
Requirements and decision evidence
-
organism: Homo sapiens — Meets requirement
- Supported by the indexed evidence.
- organism_evidence_text: Homo sapiens
-
assay type: bulk RNA-seq — Meets requirement
- Supported by the indexed evidence.
- assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed b...
-
specimen category: Tissue or biopsy — Insufficient evidence
- The required value is not reported.
-
excluded sample type excludes: cell line, organoid, xenograft — Meets requirement
- Supported by the indexed evidence.
-
specimen category excludes: Biofluid — Meets requirement
- Supported by the indexed evidence.
Source metadata
- Source name
- metastasized cancer
- Characteristics
- tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
- Description
- Not reported
- Indexed organism evidence
- REPORTED · SAMPLE_REPORTED: Homo sapiens
- Indexed assay evidence
- MAPPED_FROM_REPORTED_TEXT · SAMPLE_MAPPED: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
- Source
- GEO
Original indexed metadata
sample_accession: GSM1228237
sample_title: metastasized cancer AMC_24-3
source_name: metastasized cancer
characteristics: tissue: metastatic colorectal cancer to the liver; ajcc stage: Stage IV
description:
organism_code: HOMO_SAPIENS
organism_evidence_status: REPORTED
organism_evidence_source: SAMPLE_REPORTED
organism_evidence_text: Homo sapiens
assay_type_code: BULK_RNA_SEQ
assay_evidence_status: MAPPED_FROM_REPORTED_TEXT
assay_evidence_source: SAMPLE_MAPPED
assay_evidence_text: Total RNA was isolated by RNeasy Mini Kit (Qiagen, CA, USA), according to the manufacturer's protocol. The quality and integrity of the RNA were confirmed by agarose gel electrophoresis and ethidium bromide staining, followed by visual examination under ultraviolet light.; Sequencing library was prepared using TruSeq RNA Sample Preparation kit v2 (Illumina, CA, USA) according to the manufacturer’s protocols. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads, fragmented, and converted into cDNAs. Then, adapters were ligated and the fragments were amplified on a PCR.; Base calling was performed by Illumina Genome Studio(V2010.1).; A reference genome sequence data of Homo sapiens was obtained from University of California Santa Cruz (UCSC) Genome Browser Gateway (assembly ID: hg19). Reference genome index was built by using bowtie2-build component of Bowtie2 (ver. 2.0, http://bowtie-bio.sourceforge.net/bowtie2) and SAMtools (ver. 0.1.18, http://samtools.sourceforge.net/).; To estimate average and standard deviation of fragment size of paired-end reads, reference transcriptome was generated by MakeTranscriptome component of USeq tool (ver. 8.4.4, http://useq.sourceforge.net/). Then, generated reference transcriptome was indexed by Novoindex followed by reads mapping to transcriptome and measurements of average and standard deviation of fragment size in paired-end reads using Novoalign provided by Novocraft software (ver. 2.8.3, http://www.novocraft.com/). Tophat2 was applied to tissue samples for mapping reads to reference genome and estimated average and standard deviation of fragment size of each sample were used as parameters of Tophat2.; The fragments
per
kilobase
of
transcript
per
million
fragments
mapped (FPKM) of each sample was estimated by Cufflinks software (V2.0.2).; Genome_build: hg19; Supplementary_files_format_and_content: tab-delimited text format with FPFM values; RNA-Seq