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Sample GSM4213401 Query DataSets for GSM4213401
Status Public on Apr 14, 2021
Title Merb 30 min rep1
Sample type SRA
 
Source name retinal pigment epithelium
Organism Homo sapiens
Characteristics cell line: hTERT RPE-1
genotype/variation: wild type
treatment: Merbarone, 30 min
Treatment protocol RPE-1 cells were treated with vehicle (DMSO) for 30 minutes or merbarone (200μM) for 30 or 120 minutes.
Growth protocol RPE-1 cells were serum starved by 48h incubation in Dulbecco's Modified Eagle’s Medium (DMEM) F-12 (Sigma) supplemented with penicillin, streptomycin and 0.1% Fetal Bovine Serum (FBS) (Sigma) at 37ºC in 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated with the RNeasy kit from Qiagen following instructions from the manufacturer.
cDNA libraries were prepared with TruSeq Stranded mRNA (Illumina) using 150ng of total RNA.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Data processing Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to hg19 whole genome using bowtie v1.2.0 with parameter -m 1.
Differentially expressed genes were identified using DEseq2 (Love MI, Huber W, Anders S (2014). “Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.” Genome Biology, 15, 550. doi: 10.1186/s13059-014-0550-8).
Genome_build: hg19 (GRCh37)
Supplementary_files_format_and_content: Tab-delimited text files include RPKM values for each sample and were computed using custom R scripts that made use of the Bioconductor libraries bamsignals and edgeR.
Supplementary_files_format_and_content: bigWig files were generated using bamCoverage function from deepTools v2.4.1 with parameters --binSize 50 –normalizeUsingRPKM. Refs: Mammana A, Helmuth J (2019). bamsignals: Extract read count signals from bam files. R package version 1.18.0, https://github.com/lamortenera/bamsignals . McCarthy DJ, Chen Y, Smyth GK (2012). “Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation.” Nucleic Acids Research, 40(10), 4288-4297. doi: 10.1093/nar/gks042. Ramírez, Fidel, Devon P. Ryan, Björn Grüning, Vivek Bhardwaj, Fabian Kilpert, Andreas S. Richter, Steffen Heyne, Friederike Dündar, and Thomas Manke. deepTools2: A next Generation Web Server for Deep-Sequencing Data Analysis. Nucleic Acids Research (2016). doi:10.1093/nar/gkw257
 
Submission date Dec 10, 2019
Last update date Apr 14, 2021
Contact name Felipe Cortés Ledesma
E-mail(s) fcortes@cnio.es
Organization name CNIO
Department Molecular Oncology
Lab Topology and DNA breaks
Street address Melchor Fernández Almagro 3
City Madrid
State/province Madrid
ZIP/Postal code 28029
Country Spain
 
Platform ID GPL11154
Series (2)
GSE141799 Control of RNA polymerase II promoter-proximal pausing by DNA supercoiling [RNA-seq]
GSE141800 Control of RNA polymerase II promoter-proximal pausing by DNA supercoiling
Relations
BioSample SAMN13528539
SRA SRX7341870

Supplementary file Size Download File type/resource
GSM4213401_rna_seq_RPE_Merb_30min_1.bigWig 12.0 Mb (ftp)(http) BIGWIG
GSM4213401_rna_seq_RPE_Merb_30min_1_RPKM.txt.gz 201.7 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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