Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Blood
Cell type
MOLM-13
Primary Tissue
Blood
Tissue Diagnosis
Leukemia Acute Myelogenous

Attributes by original data submitter

Sample

source_name
Whole cell
cell line
leukemia cell line MOLM13
truseq barcode
ATCACG
genotype/variation
WT
ip antibody
IgG
antibody vendor
Abcam
antibody catalog num
ab171870
antibody lot num
GR260971

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Chromatin immunoprecipitation was performed as previously described (Dawson et al., 2009). Firstly MOLM13 cells were cross-linked with 1% formaldehyde for 10 minutes. 20*10^6 cells were used for each immunoprecipitation with 3ug of specific antibodies or IgG. Immunoprecipitated DNA was purified using the ChIP DNA purification kit (Zymo). Single end 50 bp libraries were prepared using the Bioo Scientific NEXTflex ChIP seq kit following manufacturer's recommendations. Reads were sequenced using HiSeq 1500 and multiplexed reads were split based on their barcodes using Illumina Basespace.

Sequencing Platform

instrument_model
Illumina HiSeq 1500

hg38

Number of total reads
50440020
Reads aligned (%)
94.0
Duplicates removed (%)
56.2
Number of peaks
1067 (qval < 1E-05)

hg19

Number of total reads
50440020
Reads aligned (%)
92.9
Duplicates removed (%)
58.5
Number of peaks
1089 (qval < 1E-05)

Base call quality data from DBCLS SRA