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SRX752949: GSM1538099: MC9; Homo sapiens; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 71.8M spots, 6.6G bases, 3.1Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Genome and transcriptome profiling of fibrolamellar carcinoma [RNA-Seq]
show Abstracthide Abstract
Fibrolamellar hepatocellular carcinoma (FL-HCC) is a rare variant of HCC that most frequently affects young adults. Because of its rarity and an absence of preclinical models, the molecular biology of FL-HCC remains unclear. Our objective was to analyze chromosomal alterations and dysregulated gene expression in tumor specimens collected at a single center during two decades of experience with FL-HCC. Overall design: We analyzed 38 specimens from 26 patients by array comparative genomic hybridiziation (aCGH) and 35 specimens from 16 patients by transcriptome sequencing (RNA-seq). This submission represents transcriptome component of study.
Sample: MC9
SAMN03165784 • SRS738406 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was extracted from fresh frozen tissue using the Roche High Pure FFPE kit (Roche Diagnostics). After Ribogreen quantification and quality control via Agilent BioAnalyzer, 0.5 to 1 ug of total RNA underwent stranded TruSeq library preparation according to the manufacturer's instructions (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a HiSeq 2000 in a 50bp/50bp paired-end run, using the TruSeq SBS Kit v3 (Illumina). An average of 69 million paired reads were generated per sample. Ribosomal reads represented at most 0.83% of total reads, while mRNA bases accounted for an average of 61% of reads.
Experiment attributes:
GEO Accession: GSM1538099
Links:
External link:
Runs: 1 run, 71.8M spots, 6.6G bases, 3.1Gb
Run# of Spots# of BasesSizePublished
SRR164304171,804,5886.6G3.1Gb2017-06-09

ID:
1089608

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