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Sample GSM5155758 Query DataSets for GSM5155758
Status Public on Sep 01, 2022
Title RD.R1
Sample type SRA
 
Source name RPE-1 cell line
Organism Homo sapiens
Characteristics cell line: RPE-1
treatment: DMSO
Treatment protocol Cells were treated with 0.4micromolar aphidicolin or similar volume vehicle (DMSO) as control, for 24hrs, before RNA was extracted.
Growth protocol RPE-1 and BJ cells were cultured in media (DMEM-F12 or DMEM, respectively) supplemented with 10% FBS and 100U penicillin/streptomycin, in flasks.
Extracted molecule total RNA
Extraction protocol RNA was extracted using Qiagen RNEasy kit
Library construction was performed using Lexogen 3’ tagSeq kit and RNAseq was carried out at Bart's and the London Genome Centre.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Description RPE-1 cells in DMSO replicate 1
bcc34_Log2CPM.txt
Data processing RNA-Seq reads were mapped to the human genome (hg38, Genome Reference Consortium GRCh38) using using HISAT2 version 2.1.0
Number of reads aligned to the exonic region of each gene were counted using htseq-count based on the Ensembl annotation.
Genes that achieved at least one read count per million reads (CPM) in at least 25% of the samples were kept.
Genome_build: hg38
Supplementary_files_format_and_content: tab-delimited text file includes log2 cpm values for each sample
 
Submission date Mar 10, 2021
Last update date Sep 01, 2022
Contact name Eleni Maniati
E-mail(s) e.maniati@qmul.ac.uk
Organization name Queen Mary University of London
Department Barts Cancer Institute
Lab Cancer and Inflammation
Street address John Vane Science Centre, Charterhouse Square
City London
ZIP/Postal code EC1M 6BQ
Country United Kingdom
 
Platform ID GPL18573
Series (1)
GSE168689 DNA Replication Stress Generates Distinctive landscapes of DNA copy number alterations and chromosome scale losses
Relations
BioSample SAMN18250509
SRA SRX10310881

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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