Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Blood
Cell type
Macrophages
MeSH Description
The relatively long-lived phagocytic cell of mammalian tissues that are derived from blood MONOCYTES. Main types are PERITONEAL MACROPHAGES; ALVEOLAR MACROPHAGES; HISTIOCYTES; KUPFFER CELLS of the liver; and OSTEOCLASTS. They may further differentiate within chronic inflammatory lesions to EPITHELIOID CELLS or may fuse to form FOREIGN BODY GIANT CELLS or LANGHANS GIANT CELLS. (from The Dictionary of Cell Biology, Lackie and Dow, 3rd ed.)

Attributes by original data submitter

Sample

source_name
wild type RPM mouse 1
cell type
red pulp macrophage
strain
BALB/c
genotype
Wild Type
sorting
Ly6Glo CD11blo/- F4/80hi 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
66719192
Reads aligned (%)
90.2
Duplicates removed (%)
36.8
Number of peaks
62221 (qval < 1E-05)

mm9

Number of total reads
66719192
Reads aligned (%)
90.0
Duplicates removed (%)
36.8
Number of peaks
62161 (qval < 1E-05)

Base call quality data from DBCLS SRA