Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Blood
Cell type
Monocytes
MeSH Description
Large, phagocytic mononuclear leukocytes produced in the vertebrate BONE MARROW and released into the BLOOD; contain a large, oval or somewhat indented nucleus surrounded by voluminous cytoplasm and numerous organelles.

Attributes by original data submitter

Sample

source_name
wild type splenic monocytes mouse 2
cell type
Monocyte
strain
BALB/c
genotype
Wild Type
sorting
Ly6Glo CD11bhi F4/80- cells

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
RNA-seq: Cell lysates were frozen in RLT plus buffer at -80oC prior to processing. ATAC-seq: cells were processed immediately For RNA-Seq: total RNA was extracted using the RNEasy plus micro kit (Qiagen). Cells were reuspended in RLT plus buffer and stored briefly at – 80 °C prior to extraction. All reagents, plastic ware, and supplies used were sterile, nuclease free, and of molecular biology grade. RNA purity (A260/A280>1.80) and concentration were determined using nanodrop spectrophotometer (Thermo Fisher scientific, Delaware USA). RNA integrity was studied using the 2100 Bioanalyzer System (Agilent) and RNA 6000 Nano Kit. A RNA Integrity Number (RIN) of 6.3 was the lowest cut-off for RNA Sequencing. For ATAC-seq, cells were processed immediately as described (Corces et al (2017), Nat. Methods, 14, 959) RNA-seq libraries were constructed using the Stranded total RNA-seq v2-pico kit (Takara) and ATAC-seq libraries were constructed as described (Corces et al (2017), Nat. Methods, 14, 959)

Sequencing Platform

instrument_model
Illumina NovaSeq 6000

mm10

Number of total reads
56525828
Reads aligned (%)
90.3
Duplicates removed (%)
23.3
Number of peaks
58246 (qval < 1E-05)

mm9

Number of total reads
56525828
Reads aligned (%)
90.1
Duplicates removed (%)
23.4
Number of peaks
58190 (qval < 1E-05)

Base call quality data from DBCLS SRA