GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Series GSE62492 Query DataSets for GSE62492
Status Public on Feb 08, 2015
Title Genome wide analysis of AR binding sites and histone modifications in prostate cancer
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Prostate cancer is the most common cancer in men and AR downstream signalings promote prostate cancer cell proliferation.We performed ChIP-seq analysis to investigate the role of AR and histone modifications.In addition, by siRNA mediated knockdown of AR-associated factors, changes of AR-binding sites in prostate cancer cells were analyzed..
Overall design ChIP-sequence analysis of AR and its associated factors in prostate cancer cells
Contributor(s) Takayama K, Inoue S, Tsutsumi S, Aburatani H
Citation(s) 25537508, 31454442
Submission date Oct 20, 2014
Last update date Nov 12, 2019
Contact name Ken-ichi Takayama
Organization name Tokyo Metropolitan Institute of Gerontology
Street address Sakaecho
City Itabashi-ku
ZIP/Postal code 173-0015
Country Japan
Platforms (1)
GPL10999 Illumina Genome Analyzer IIx (Homo sapiens)
Samples (23)
GSM1527822 lncap_AR_vehicle
GSM1527823 lncap_R1881_24h_AR
GSM1527824 lncap_vehicle_AcH3
BioProject PRJNA264289
SRA SRP049047

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE62492_RAW.tar 388.8 Mb (http)(custom) TAR (of BAR, TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap