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Sample GSM2186466 Query DataSets for GSM2186466
Status Public on Oct 05, 2016
Title AR G2/M ChIP-Seq
Sample type SRA
 
Source name LNCaP Cell Line
Organism Homo sapiens
Characteristics cell line: LNCaP
cell cycle arrest treatment: 2μg/mL aphidicolin for 15 hours, followed by washout and treatment with 50ng/mL nocodozole for 9 hours +3 hour 10nm DHT
dht treatment: +
chip antibody: AR N-20 (SC-816)
Treatment protocol Cells were treated with indicated drug 24 hours prior to harvest, and 10nM DHT 3 hours prior to harvest, with the exception of G0 control which was treated with CDT for 72 hours and EtOH 3 hours prior to harvest
Growth protocol LNCaP cells were cultured in hormone proficient media unless otherwise indicated.
Extracted molecule genomic DNA
Extraction protocol ChIP was performed as previously described by Schmidt et al 2009
Illumina library prep kit was utilyzed according to manufacturer's instructions
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer IIx
 
Data processing alignment to hg18 genome with bowtie
peak calling with MACS1.4 with a 10E-8 p-value cutoff
Genome_build: hg18
Supplementary_files_format_and_content: BED file with called peaks
 
Submission date Jun 02, 2016
Last update date May 15, 2019
Contact name Christopher McNair
E-mail(s) christopher.mcnair@jefferson.edu
Organization name Thomas Jefferson University
Department Medical Oncology
Street address 833 Chestnut Street Ste 1140
City Philadelphia
State/province PA
ZIP/Postal code 19107
Country USA
 
Platform ID GPL10999
Series (2)
GSE82202 Identification of cell cycle regulated, DHT induced AR binding events
GSE82203 Identification of DHT induced cell cycle dependent trascriptome and AR binding events
Relations
BioSample SAMN05199936
SRA SRX1818077

Supplementary file Size Download File type/resource
GSM2186466_AR_LNCaP_G2_M_peaks.1E-8.bed.gz 524.6 Kb (ftp)(http) BED
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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