Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Adipocyte
Cell type
Subcutaneous adipocytes
NA
NA

Attributes by original data submitter

Sample

source_name
subcutaneous gluteofemoral fat
body type
apple
cell type
adipocytes
fat depot
subcutaneous gluteofemoral fat
Sex
female

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Fat biospsies were collected, adipocytes were isolated by centrifugation. Nuclei were used for tagmentation using Nextera DNA Library Preparation Kit (Illumina).DNA was purified with MinElute PCR Purification Kit (Qiagen). Tagmented DNA was amplified with Kapa HiFi Hot Start Kit (Kapa Biosystems) using 16 PCR cycles. Amplified libraries were purified with Agencourt AMPure XP (Beckman Coulter). Fragment distribution of libraries was assessed with Agilent Bioanalyzer.

Sequencing Platform

instrument_model
Illumina HiSeq 2500

hg38

Number of total reads
24067065
Reads aligned (%)
98.3
Duplicates removed (%)
38.5
Number of peaks
2512 (qval < 1E-05)

hg19

Number of total reads
24067065
Reads aligned (%)
97.8
Duplicates removed (%)
39.5
Number of peaks
2440 (qval < 1E-05)

Base call quality data from DBCLS SRA