Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Blood
Cell type
CAR-T cells
NA
NA

Attributes by original data submitter

Sample

source_name
Primary human T cells engineered with CD19 CAR
cell type
Primary human T cells engineered with CD19 CAR
treatment condition
15day exposure to BIDko Nalm6

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
cells were processed following the Omni ATAC-seq protocol. To isolate nuclei, cells were washed 2x with ice-cold PBS followed by resuspension in ATAC- resuspension buffer containing 0.1% NP40, 0.1% Tween-20 and 0.01% Digitonin. Cells were incubated on ice for 3 minutes and washed out with ATAC- resuspension buffer containing (0.1% Tween20). Nuclei were pelleted and transposed with Tn5 transposase. nuclei were isolated from 50,000 sorted CART19 cells, followed by the transposition reaction using Tn5 transposase (Illumina) for 30 minutes at 37°C with 1000rp mixing.  Purification of transposed DNA was completed with DNA Clean and Concentrator (Zymo) and fragments were barcoded with ATAC-seq indices.  Final libraries were double size selected using AMPure beads prior to sequencing.

Sequencing Platform

instrument_model
NextSeq 500

hg38

Number of total reads
60000564
Reads aligned (%)
96.4
Duplicates removed (%)
33.3
Number of peaks
51165 (qval < 1E-05)

hg19

Number of total reads
60000564
Reads aligned (%)
95.7
Duplicates removed (%)
33.7
Number of peaks
50925 (qval < 1E-05)

Base call quality data from DBCLS SRA