Sample information curated by ChIP-Atlas

Antigen

Antigen Class
TFs and others
Antigen
AR

Cell type

Cell type Class
Prostate
Cell type
Prostate cancer
NA
NA

Attributes by original data submitter

Sample

source_name
Prostate Cancer
treatment
R-9b inhibitor treatment
cell type
Prostate Cancer Cell Line
chip antibody
acK609-AR antibody

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
The lysates were immunoprecipitation with acK609-AR antibodies (2 ug) for overnight. Ten nanograms of immunoprecipitated DNA was fragmented to 300 base pairs using a Covaris M220 Focused-ultrasonicator (Covaris, Inc., Woburn, MA) and then used to generate sequencing libraries using the Kapa Hyper Prep Kit (Roche Sequencing Solutions Inc., Pleasanton, CA). The size and quality of the library was evaluated using the Agilent BioAnalyzer (Agilent Technologies, Inc., Santa Clara, CA), and the library was quantitated with the Kapa Library Quantification Kit. Each enriched DNA library was then sequenced on an Illumina NextSeq 500 sequencer to generate 40-50 million 75-base paired-end reads (Illumina, Inc., San Diego, CA). The raw sequence data were aligned using BowTie 2 [1], and the binding sites were identified using the MACS peak-finding software

Sequencing Platform

instrument_model
Illumina HiSeq 3000

hg38

Number of total reads
38774868
Reads aligned (%)
91.7
Duplicates removed (%)
2.4
Number of peaks
1122 (qval < 1E-05)

hg19

Number of total reads
38774868
Reads aligned (%)
90.6
Duplicates removed (%)
2.5
Number of peaks
658 (qval < 1E-05)

Base call quality data from DBCLS SRA