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Sample GSM1375519 Query DataSets for GSM1375519
Status Public on May 09, 2014
Title NT-2
Sample type SRA
 
Source name Human cervical cancer
Organism Homo sapiens
Characteristics cell line: HeLa
time: control
treatment: untreated
Treatment protocol Cells were treated with DRB for 3hr and harvested after DRB removal. Cells were also labeld with 4sU for 8 min beofre harvested.
Growth protocol HeLa cells were grown in DMEM supplemented with 10% heat-inactivated fetal bovine serum and penicillin-streptomycin antibiotics solution
Extracted molecule total RNA
Extraction protocol 4sU labled RNA was tagged with Biotion, and enriched with Streptavidin magnetic beads.
cDNA libraries were prepared with Illumina TruSeq RNA sample preparation v2 kit according to the manufacturer's instructions but without the polyA isolation stage
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description Nascent RNA labled with 4sU
Data processing All reads were aligned to the human reference genome (hg19, GRCh37) using the bowtie 2 aligner with default parameters (only setting –N 1)
For each experiment we constructed a genome-wide profile of the signal per disjoint 100 bp adjacent bins. The sum of each experiment was normalized to be 106
Genome_build: hg19
Supplementary_files_format_and_content: xlsx file describe the transcription elongation velocity measured for all DRB-dependent genes.
 
Submission date Apr 26, 2014
Last update date May 15, 2019
Contact name Gilad Fuchs
E-mail(s) gilad.fuchs@weizmann.ac.il
Organization name Weizmann Institute of Science
Street address Rehovot
City Rehovot
ZIP/Postal code 71600
Country Israel
 
Platform ID GPL16791
Series (1)
GSE57116 4sUDRB-seq: measuring transcription elongation and initiation genomewide
Relations
BioSample SAMN02737861
SRA SRX528190

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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