|
Status |
Public on Apr 12, 2017 |
Title |
ChIP-seq for FOXO3 [SL16038] |
Sample type |
SRA |
|
|
Source name |
HepG2
|
Organism |
Homo sapiens |
Characteristics |
cell line: HepG2 antibody (clone id#) used: R5.2.1B7
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Exponentially growing cells from ENCODE Tier 1 and Tier 2 cell lines were crosslinked in 1% formaldehyde and harvested in batches of 20 million cells per replicate. Prepared nuclei were resuspended in RIPA buffer and chromatin shearing was performed on a Bioruptor Twin instrument (Diagenode). Antibody (5 µg/rxn) was coupled to M-280 Dynabeads (ThermoFisher Scientific; 11201) overnight prior to addition of sheared chromatin. A small aliquot of the sheared chromatin was reserved as an input control. Following incubation and wash steps, captured chromatin and input control were reverse crosslinked overnight at 65°C and recovered using the QIAquick PCR Purification System (Qiagen; 28104). ChIP-seq libraries (illumina) were prepared and run on an Illumina HiSeq 2500 instrument.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
CHIP-seq reads were aligned to hg19-female using Bowtie2 with default parameters Peaks were called using MACS2 with default parameters Genome_build: hg19-female Supplementary_files_format_and_content: bed (narrowPeak) files were generated using macs2
|
|
|
Submission date |
Apr 11, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Anand Venkataraman |
E-mail(s) |
avenka11@jhu.edu
|
Phone |
4105021871
|
Organization name |
Johns Hopkins University
|
Department |
Neuroscience
|
Lab |
Seth Blackshaw
|
Street address |
733 N Broadway, MRB 322
|
City |
Baltimore |
State/province |
MD |
ZIP/Postal code |
21205 |
Country |
USA |
|
|
Platform ID |
GPL16791 |
Series (1) |
GSE97661 |
Testing mAbs generated by the PCRP pipeline in ChIP-seq application |
|
Relations |
BioSample |
SAMN06710669 |
SRA |
SRX2733452 |