Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Lung
Cell type
1153
NA
NA

Attributes by original data submitter

Sample

source_name
lung
cell line
1153
chip-antibody
None

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
The tissue homogenate was filtered with a 70 µm cell strainer and fixed in 1% formaldehyde at room temperature for 10 min. The tissue pellet was collected through centrifugation, washed twice with cold PBS and then incubated with lysis buffer on ice for 20 min. The tissue lysate was sonicated, and DNA was sheared to an average size of 100-300 bp. Approximately 10% of the total tissue lysate was collected as input, while the other portion was first precleared with uncoupled Protein-A Dynabeads (Novex, 10002D) and incubated with H3K27ac-coupled Protein-A Dynabeads for 6 hours in a cold room. Then, the Dynabeads were collected using a magnet track, and chromatin was eluted. The DNA was then processed for NGS library construction and sequenced.

Sequencing Platform

instrument_model
HiSeq X Ten

hg38

Number of total reads
92938330
Reads aligned (%)
81.2
Duplicates removed (%)
21.8
Number of peaks
2608 (qval < 1E-05)

hg19

Number of total reads
92938330
Reads aligned (%)
80.0
Duplicates removed (%)
22.5
Number of peaks
772 (qval < 1E-05)

Base call quality data from DBCLS SRA