Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Blood
Cell type
CD34+
NA
NA

Attributes by original data submitter

Sample

source_name
CD34 Culture
cell type
Erythroid
day of differentiation
Day 13
gender
female
differentiation protocol
P1

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Assay for transposition of active chromatin sequencing (ATAC-Seq) was performed as previously published (Buenrostro, 2013) on single cell suspensions. 60000-80000 cells were used per biological replicate. Cells were lysed and nuclei were isolated prior to transposition with Tn5 transposase (Nextera, Illumina) for 30 minutes at 37°C. DNA was purified using a MinElute kit (Qiagen). Libraries were amplified and barcoded using the NEBNext 2xMastermix (NEB) and the custom primers as published in Buenrostro et al., 2013.ATAC-Seq libraries profiles were visualized using D1000 tape on the Tapestation (Agilent). The libraries were quantified using the universal library quantification kit (KAPA Biosystems).

Sequencing Platform

instrument_model
NextSeq 500

hg38

Number of total reads
69322641
Reads aligned (%)
93.7
Duplicates removed (%)
78.8
Number of peaks
16243 (qval < 1E-05)

hg19

Number of total reads
69322641
Reads aligned (%)
93.5
Duplicates removed (%)
78.8
Number of peaks
16131 (qval < 1E-05)

Base call quality data from DBCLS SRA