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SRX4634268: GSM3373921: GPY231 Rep2 [RNA]; Homo sapiens; RNA-Seq
1 ILLUMINA (HiSeq X Ten) run: 56.6M spots, 17G bases, 6.6Gb downloads

Submitted by: NCBI (GEO)
Study: Human Adipocytes Regulate Gene Expression in Triple-negative Breast Cancer Assessed by NGS Sequencing
show Abstracthide Abstract
Adipocyte was found play a pivotal role in tumorgenesis, progression and metastasis in breast cancer. However, affection of adipocyte on gene expression profile in triple-negative breast cancer (TNBC) is still not clear. In the present study, firstly we reported the gene expression profiles of TNBC regulated by human adipocytes using NGS. TNBC cell MDA-MB-231 was used in this study. MDA-MB-231 cells were treated with medium derived from adipocytes culture supernatants. Using two different RNA libraries, we sequenced the complete transcriptome(including mRNA, lncRNA, circleRNA and small RNA) of MDA-MB-231 treated with medium derived from adipocytes culture supernatants. Overall design: NGS sequencing of wild type and adipocyte treated MDA-MB-231 cells, and identifing differentiated expressed genes
Sample: GPY231 Rep2 [RNA]
SAMN09948058 • SRS3734894 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: TRIZOL reagent (Invitrogen) was used to extract total RNA from cells following the manufacturer's protocols. First, Total RNA was treated with the Epicentre Ribo-Zero kit (cat.#MRZH11124) to remove the all the rRNAs. The remaining RNAs were processed using the TruSeq RNA Sample Prep Kit according to the Illumina protocol. After cDNA synthesis, 6.5 pmol of DNA from each sample were clustered and sequenced on the Illumina HiSeq X-Ten (Illumina) in 150 bp paired-end reads.
Experiment attributes:
GEO Accession: GSM3373921
Links:
Runs: 1 run, 56.6M spots, 17G bases, 6.6Gb
Run# of Spots# of BasesSizePublished
SRR777912156,564,52117G6.6Gb2018-09-25

ID:
6260971

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