Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Blood
Cell type
Th1 Cells
MeSH Description
A subset of helper-inducer T-lymphocytes which synthesize and secrete INTERLEUKIN-2; INTERFERON-GAMMA; and INTERLEUKIN-12. Due to their ability to kill antigen-presenting cells and their lymphokine-mediated effector activity, Th1 cells are associated with vigorous delayed-type hypersensitivity reactions.

Attributes by original data submitter

Sample

source_name
mouse in-vitro activated Th1 cells
strain
C57BL/6
culture condition
6 days in vitro culture
genotype
Ifng-as1 KO
tissue
mouse in-vitro activated Th1 cells

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
ATAC-seq was performed according to a published protocol (Buenrostro et al., 2013) with minor modification. Fifty thousand cells were pelleted and washed with 50 μl 1× PBS, followed by treatment with 50 μl lysis buffer (10 mM Tris-HCl [pH 7.4], 10 mM NaCl, 3 mM MgCl2, 0.1% IGEPAL CA-630). After pelleting the nuclei by centrifuging at 500 × g for 10 min, the pellets were re-suspended in a 40-μl transposition reaction with 2 μl Tn5 transposase (FC-121-1030; Illumina) to tag and fragmentalize accessible chromatin. The reaction was incubated at 37°C with shaking at 300 rpm for 30 min. The fragmentalized DNAs were then purified using a QIAGEN MinElute kit and amplified with 10 or 11 cycles of PCR based on the amplification curve. Libraries were purified using a QIAGEN PCR cleanup kit. Libraries were sequenced for 75 cycles (paired-end reads) on a Illumina HiSeq 2500.

Sequencing Platform

instrument_model
Illumina HiSeq 2500

mm10

Number of total reads
50826506
Reads aligned (%)
89.7
Duplicates removed (%)
28.5
Number of peaks
24385 (qval < 1E-05)

mm9

Number of total reads
50826506
Reads aligned (%)
89.6
Duplicates removed (%)
28.7
Number of peaks
24339 (qval < 1E-05)

Base call quality data from DBCLS SRA