Sample information curated by ChIP-Atlas

Antigen

Antigen Class
No description
Antigen
NA

Cell type

Cell type Class
Blood
Cell type
BLaER1
NA
NA

Attributes by original data submitter

Sample

ENA first public
2019-01-01
ENA last update
2018-08-03
ENA-CHECKLIST
ERC000011
External Id
SAMEA4814084
INSDC center alias
Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Bioinformatics and Genomics.
INSDC center name
Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Bioinformatics and Genomics.
INSDC first public
2019-01-01T17:01:59Z
INSDC last update
2018-08-03T09:09:15Z
INSDC status
public
Submitter Id
E-MTAB-7114:Human_012h Input replicate 2
broker name
ArrayExpress
cell line
BLaER1
cell type
B cell
common name
human
disease
Epstein-Barr virus-related Burkitts lymphoma
organism part
blood
sample name
E-MTAB-7114:Human_012h Input replicate 2

Sequenced DNA Library

library_name
Human_012h Input replicate 2_s
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
BLaER1 cells are as described here: https://doi.org/10.1016/j.celrep.2013.03.003 and are derived as a subclone of Seraphina cells CVCL_M646. Cells were collected after 12 hours of transdifferentiation. To track the transdifferentiation process along the 7 days it lasts, fluorescent staining of cell surface markers was done with antibodies against Mac1 (APC) and CD19 (APC-Cy7) (BD Pharmigen). Samples were analyzed on the LSRII flow cytometer (BD Biosciences) and data were analyzed with FlowJo software (Tree Star). Human BLaER1 cells and mouse C10 cells were grown in RPMI (Invitrogen) supplemented with 10% heat-inactivated fetal bovine serum, 2 mM L-glutamine, and 100 U/ml penicillin G sodium. Transdifferentiation was induced in BlaER1 by addition of 100nM of β-estradiol (Calbiochem) and grown with 10nM of IL-3 and CSF-1 (Peprotech). Cells were crosslinked with 1% formaldehyde for 10 minutes at room temperature and sheared with a Covaris sonicator. 5 μg of chromatin and 5 μg of antibody against rat CEBPA (sc-61 X, Santa Cruz) were incubated in RIPA buffer (140 mM NaCl, 10 mM Tris HCl pH 8.0, 1 mM EDTA, 1 % Triton X-100, 0.1 % SDS, 0.1 % Na deoxycholate, protease inhibitors). DNA libraries were prepared with 1 ng of purified ChIP using NEBNext DNA Library kit for Illumina following the manufacturer's protocol.

Sequencing Platform

instrument_model
Illumina HiSeq 2000

hg38

Number of total reads
90875655
Reads aligned (%)
98.5
Duplicates removed (%)
4.6
Number of peaks
1661 (qval < 1E-05)

hg19

Number of total reads
90875655
Reads aligned (%)
97.6
Duplicates removed (%)
6.2
Number of peaks
1591 (qval < 1E-05)

Base call quality data from DBCLS SRA