Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Blood
Cell type
Erythroblasts
MeSH Description
Immature, nucleated ERYTHROCYTES occupying the stage of ERYTHROPOIESIS that follows formation of ERYTHROID PRECURSOR CELLS and precedes formation of RETICULOCYTES. The normal series is called normoblasts. Cells called MEGALOBLASTS are a pathologic series of erythroblasts.

Attributes by original data submitter

Sample

source_name
primitive erythroblasts
embryonic day
E10.5
tissue
Peripheral Blood
genotype
setd8-null

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Primitive erythroblasts were removed from peripheral blood by dissection in PBS supplemented with glucose and BSA Briefly, nuclei were collected from Setd8 null and control erythroblats following cell lysis and subjected to tagmentation using transpoase (Ilumina Nextera FC121-1030). Samples were then amplified x 5 PCR cycles [980C/45s + 5 x (980C/15s + 630C/30s + 720C/30s) + 720C/1min] using KAPA HiFi HotStart ReadyMix PCR Kit (KK2601/KK2602) and cleaned with Qiagen MiniElute column. The library was then amplified with PCR [980C/45s + Y x (980C/15s + 630C/30s + 720C/30s) + 720C/1min], with the number of cycles (Y) determined through via a qPCR library amplification test. The resulting PCR producte was cleaned using Agencourt AMPure XP magnetic beads (Beckman Coulter A63880)

Sequencing Platform

instrument_model
Illumina HiSeq 2500

mm10

Number of total reads
31480210
Reads aligned (%)
67.1
Duplicates removed (%)
96.2
Number of peaks
1244 (qval < 1E-05)

mm9

Number of total reads
31480210
Reads aligned (%)
67.0
Duplicates removed (%)
96.3
Number of peaks
1225 (qval < 1E-05)

Base call quality data from DBCLS SRA