|
Status |
Public on Jan 05, 2016 |
Title |
EBNA3A_ChIP-Seq |
Sample type |
SRA |
|
|
Source name |
Lymphoblast Cell Lines
|
Organism |
Homo sapiens |
Characteristics |
cell line: Epstein Barr Virus transformed Lymphoblast Cell Line genotype/variation: expressing HA tagged EBNA3A protein chip antibody: HA-probe Antibody F-7 (sc-7392; Santa Cruz)
|
Treatment protocol |
Cells were fixed with 1% formaldehyde. After wash with twice PBS, the cells were lyzed in ChIP lysis buffer. Lysates were sonicated and cleared by centrifugation. HA antibody F-7 (sc-7392; Santa Cruz) was incubated with the lysate overnight at 4ÂșC.
|
Growth protocol |
Cells were grown in RPMI media supplemented witth 10%fetal bovine serum, penicillin and streptomycin.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Protein A/G magnetic beads was used to capture the protein DNA complexed. The eluted protein-DNA complexes were reverse crosslinked and DNA was purified by a QIAquick PCR purification kit (28706; Qiagen). Libraries were prepared using PrepX BeadX kit from IntegenX. Briefly, DNA was end-repaired. 3' A base was added and ligated to adaptors. After PCR amplification, DNA was purified and analyzed with Illumina HiSeq.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Basecalls performed by the Harvard Medical School Biopolymer facility as per Illumina recommendations ChIP-seq reads were aligned to the human hg19 genome assembly using Bowtie (http://bowtie-bio.sourceforge.net/index.shtml) peaks were called using MOSAiCS (MOdel-based one and two Sample Analysis and inference for ChIP-Seq Data) controlling the false discovery rate (FDR) at 0.05. Genome_build: hg19 and V01555.2 Supplementary_files_format_and_content: wig files were generated using MOSAiCS; Scores represent read counts
|
|
|
Submission date |
Dec 18, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Eric Johannsen |
E-mail(s) |
ejohannsen@medicine.wisc.edu
|
Organization name |
UW-Madison
|
Department |
Department of Medicine
|
Street address |
1111 Highland Ave
|
City |
Madison |
State/province |
Wisconsin |
ZIP/Postal code |
53705 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE76166 |
EBNA3 proteins regulate EBNA2 binding to distinct RBPJ genomic sites |
|
Relations |
BioSample |
SAMN04351193 |
SRA |
SRX1491920 |