Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Pluripotent stem cell
Cell type
hESC derived mesodermal cells
NA
NA

Attributes by original data submitter

Sample

source_name
ATAC Library MES
cell line
RUES2
cell type
mesodermal cells (MES)
time point
Day 2 of differentiation

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
ATAC-seq was performed according to the protocol from Buenrostro et al. (2015). Briefly cells were harvested from cell culture and lysed in lysis buffer (10mM Tris-Cl, pH 7.4, 10mM NaCl, 3mM MgCl2, 0.1% Igepal CA-630, 1x Protease inhibitor, Sigma). After lysis 5x10^4 nuclei were washed in lysis buffer and resuspended in 25ml TD buffer, 24ml Lysis buffer, 1ml TDE1 enzyme from the Nextera DNA Prep kit (Illumina FC-121-1030). The reaction was incubated for 30min at 55° and DNA was then extracted with a MinElute PCR Purfication kit (Qiagen 28004). DNA was amplified for using NEBNext High-Fidelity 2x Master Mix (M0541L) and quantified with a Qubit. All samples were pooled with Nextera primers and sequenced on an Illumina NEXTSEQ.

Sequencing Platform

instrument_model
NextSeq 500

hg38

Number of total reads
48720815
Reads aligned (%)
97.8
Duplicates removed (%)
34.2
Number of peaks
41641 (qval < 1E-05)

hg19

Number of total reads
48720815
Reads aligned (%)
97.5
Duplicates removed (%)
34.5
Number of peaks
41568 (qval < 1E-05)

Base call quality data from DBCLS SRA