Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Unclassified
Cell type
Unclassified
NA
NA

Attributes by original data submitter

Sample

source_name
Nr1h3 flox/flox
strain
Nr1h3 flox/flox
treatment1
No treatment

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Approximately 50,000 cells were washed once with PBS and once with cold lysis buffer (10 mM Tris-HCl, pH 7.4, 10 mM NaCl, 3 mM MgCl2, 0.1% IGEPAL CA-630). Cells were then suspended in 50 µl 1X reaction buffer (25μl Tagment DNA Buffer, 2.5μl Tagment DNA enzyme I, and 22.5μl water) (Nextera DNA Library Preparation Kit, Illumina). Transposase reactions were carried out at 37°C for 30 minutes and immediately DNA was purified using ChIP DNA Clean & Concentrator kits (Zymo Research). DNA was amplified using the Nextera primer Ad1 and a unique Ad2.n barcoding primer using NEBNext High-Fidelity 2XPCR Master Mix (NEB) for 14 cycles. Resulting libraries were size selected by gel excision to 175-225 bp and purified.

Sequencing Platform

instrument_model
Illumina HiSeq 4000

mm10

Number of total reads
25264397
Reads aligned (%)
96.5
Duplicates removed (%)
43.3
Number of peaks
44597 (qval < 1E-05)

mm9

Number of total reads
25264397
Reads aligned (%)
96.4
Duplicates removed (%)
43.3
Number of peaks
44604 (qval < 1E-05)

Base call quality data from DBCLS SRA