Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Blood
Cell type
CD8+ T cells
NA
NA

Attributes by original data submitter

Sample

source_name
CD8 T cells
background strain
C57BL/6
treatment
LCMV Clone 13 infection

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Lysates were centrifuge (750xg, 10min, 4oC) and nuclei were resuspended in 50μl of transposition reaction mix (TD buffer [25μl], Tn5 Transposase [2.5μl], nuclease-free water [22.5μl]; (Illumina)) and incubated for 30min at 37oC. Transposed DNA fragments were purified using a Qiagen Reaction MiniElute Kit, barcoded with NEXTERA dual indexes (Illumina) and amplified by PCR for 11 cycles using NEBNext High Fidelity 2x PCR Master Mix (New England Biolabs). PCR products were purified using a PCR Purification Kit (Qiagen) and amplified fragments size was verified on a 2200 TapeStation (Agilent Technologies) using High Sensitivity D1000 ScreenTapes (Agilent Technologies). Libraries were quantified by qPCR using a KAPA Library Quant Kit (KAPA Biosystems).

Sequencing Platform

instrument_model
NextSeq 550

mm10

Number of total reads
8407963
Reads aligned (%)
80.2
Duplicates removed (%)
29.1
Number of peaks
6873 (qval < 1E-05)

mm9

Number of total reads
8407963
Reads aligned (%)
80.2
Duplicates removed (%)
29.1
Number of peaks
6843 (qval < 1E-05)

Base call quality data from DBCLS SRA