Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Unclassified
Antigen
Unclassified

Cell type

Cell type Class
Pluripotent stem cell
Cell type
iPS cells
NA
NA

Attributes by original data submitter

Sample

source_name
hiPSC1 1.8-1.2 subline
cell line
HUES9 hESC subline

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Cells were fixed with 2mM disuccinimidyl glutarate (DSG) for 45 mins and 1% formaldehyde for 10mins, and followed by glycine for 5 mins. Chromatin DNA was sheared to 200–500 bp average in size by sonication and chromatin was immunoprecipitated with antibodies. Protein A/G beads Sigma were added and incubated overnight at 4°C. After washing and elution, the protein–DNA complex was reverse-crosslinked by heating at 65°C, and immunoprecipitated DNA was purified by using QIAquick Spin column. ChIP-seq libraries were prepared using the KAPA Library Preparation Kit (KK8201)

Sequencing Platform

instrument_model
Illumina HiSeq 4000

hg38

Number of total reads
25063521
Reads aligned (%)
88.2
Duplicates removed (%)
2.1
Number of peaks
19684 (qval < 1E-05)

hg19

Number of total reads
25063521
Reads aligned (%)
87.4
Duplicates removed (%)
3.3
Number of peaks
19496 (qval < 1E-05)

Base call quality data from DBCLS SRA