Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Neural
Cell type
Visual Cortex
MeSH Description
Area of the OCCIPITAL LOBE concerned with the processing of visual information relayed via VISUAL PATHWAYS.

Attributes by original data submitter

Sample

source_name
Adult_VsCTX_VIPcre_Input_ATAC
background
C57BL/6
genotype
Vip-cre; Sun1
tissue
Visual cortex
neuronal subtype
Mix

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
INTACT-purified nuclei were resuspended in L1 buffer (50mM Hepes pH7.5, 140mM NaCl, 1mM EDTA, 1mM EGTA, 0.25% Triton X-100, 0.5% NP40, 10% Glycerol, protease inhibitors, sodium butyrate), and centrifuged at 2000 rpm at 4°C. L1 buffer was removed, and INTACT-purified nuclei were incubated with Tn5 in TD buffer (Illumina) for 30 minutes at 37°C. To control for potential biases for Tn5 towards specific sequence compositions, we performed the above assay on naked genomic DNA isolated from cortices. Adapter-ligated DNA fragments were purified using the Qiagen MinElute kit, and subsequently PCR-amplified with the Nextera DNA sample kit using the following conditions: (1) 5 minutes at 72°C, (2) 1 minute at 98°C, (3) 15 seconds at 98°C, (4) 30 seconds at 63°C, (5) one minute at 72°C, (6) Go to step 3 eleven times, (7) hold at 10°C. All ATAC-seq libraries were sequenced on a Nextseq 500.

Sequencing Platform

instrument_model
NextSeq 500

mm10

Number of total reads
34689337
Reads aligned (%)
98.9
Duplicates removed (%)
35.0
Number of peaks
109381 (qval < 1E-05)

mm9

Number of total reads
34689337
Reads aligned (%)
98.8
Duplicates removed (%)
35.0
Number of peaks
109425 (qval < 1E-05)

Base call quality data from DBCLS SRA