Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Unclassified
Antigen
Unclassified

Cell type

Cell type Class
Blood
Cell type
Pro-B cells
NA
NA

Attributes by original data submitter

Sample

source_name
v-Abl transformed pro-B cell line
cell type
v-Abl transformed pro-B cell line
genotype
JH-del, dCas9 expressing, Emu-Bcl2, RAG2 deficient

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Crosslinked cells were treated with cell lysis buffer (5mM PIPES pH 8, 85mM KCl, 0.5% NP-40) and nuclei lysis buffer (50mM TrisCl pH 8.1, 10mM EDTA, 1% SDS) and subjected to sonication. IP and Input DNA were de-crosslinked at 65o overnight and purified via Qiagen PCR purification columns. Libraries were prepared via the TruSeq ChIP Library Preparation Kit (IP-202-1012).

Sequencing Platform

instrument_model
Illumina HiSeq 2500

mm10

Number of total reads
41949919
Reads aligned (%)
98.4
Duplicates removed (%)
25.0
Number of peaks
43011 (qval < 1E-05)

mm9

Number of total reads
41949919
Reads aligned (%)
98.3
Duplicates removed (%)
25.1
Number of peaks
42980 (qval < 1E-05)

Base call quality data from DBCLS SRA