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Sample GSM991665 Query DataSets for GSM991665
Status Public on Aug 25, 2012
Title Input
Sample type SRA
 
Source name IMR90 Human Fetal Lung Fibroblast cell line
Organism Homo sapiens
Characteristics cell line: IMR90
sample type: none
treatment: none
Treatment protocol imr90 cells were infected with ER-Ras vector and indicated hairpins. The cells were collected 4 days after tamoxifen treatment. The ChIP experiments were done as previously described (Chicas et al. 2010).
Extracted molecule genomic DNA
Extraction protocol update
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer
 
Description Input from senescent cells
Data processing The immunoprecipitated DNA was prepared for Illumina sequencing as described (Chicas et al. 2010).
The Illumina GA sequencing tags were mapped to the unmasked human reference genome (NCBI version 36, hg18) using the program Bowtie with the parameter setting ‘‘-t -q -a –best –strata -m 1.’’
ChIP-seq peak regions were determined using MACS (Zhang et al. 2008) to find ChIP-enriched regions compared with the input DNA control with default parameter settings and a significance threshold (P<1e-5).
We associated ChIP-enriched regions to a target gene if it localized within the region from 3 kb upstream of to 1 kb downstream from the transcription start site of the gene. The gene coordinates were extracted according to RefSeq gene annotation (hg18) downloaded from the University of California at Santa Cruz Genome Browser.
Genome_build: hg18
 
Submission date Aug 23, 2012
Last update date May 15, 2019
Contact name Ozlem Aksoy
E-mail(s) merto@mskcc.org
Phone 917-930-1718
Organization name CSHL
Department Watson School of Biological Sciences
Lab Scott Lowe's lab
Street address 415 East 68th Street
City New York
State/province NY
ZIP/Postal code 10065
Country USA
 
Platform ID GPL9052
Series (1)
GSE40343 Genome wide maps of E2F7 binding in IMR90 cells
Relations
SRA SRX180829
BioSample SAMN01129815

Supplementary data files not provided
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