|
Status |
Public on Nov 01, 2017 |
Title |
22Rv1_Veh_HNF4G IP |
Sample type |
SRA |
|
|
Source name |
22rV1HNF4Gs_HNF4G IP
|
Organism |
Homo sapiens |
Characteristics |
hnf4g status: wildtype ip: HNF4G cell line: 22Rv1
|
Treatment protocol |
Cells were harvested in log phase growth
|
Growth protocol |
Cells were grown in 10% FBS
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Chromatin was isolated and sheared. Following antibodies were used; HNF4G (Sigma; HPA005438 or Proteintech; 25801-1-AP); H3K4me1 (Abcam; ab8895); H3K27ac (Abcam; ab4729); AR (Abcam, ab108341); FOXA1 (Abcam; ab5089). Magnetic protein A/G beadswere used to collect immunoprecipitates. The immunoprecipate was washed and eluted using standing conditions. Purified ChIP DNA was blunt-ended, ligated to adaptors, amplified with 8-12-cycles of PCR, and sequenced.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
The sequenced reads from fastq files were mapped to hg19 using Bowtie 1.0 Peaks were called using MACS2. Downstream analysis were performed using Homer and SeqMiner Genome_build: Hg19 Supplementary_files_format_and_content: ENCODE narrowPeak: Narrow (or Point-Source) Peaks format. See https://genome.ucsc.edu/FAQ/FAQformat.html
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|
|
Submission date |
Aug 12, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Shipra Shukla |
E-mail(s) |
shuklas@mskcc.org
|
Organization name |
MSKCC
|
Street address |
417 East 68th Street
|
City |
New York |
State/province |
NY |
ZIP/Postal code |
10065 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (2) |
GSE85558 |
HNF4G, AR, FOXA1, H3K4me1, H3K27acetyl binding sites upon knockdown and overexpression of HNF4G in 22Rv1 and LNCaP prostate cancer cells respectively |
GSE85559 |
Expression profiling and occupancy after knockdown or over-expression of HFN1A or HNF4G in prostate cancer cells |
|
Relations |
BioSample |
SAMN05570468 |
SRA |
SRX2017944 |