|
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 |