Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Breast
Cell type
MDA-MB-231
Primary Tissue
Breast
Site of Extraction
Effusion, Pleural
Tissue Diagnosis
Adenocarcinoma

Attributes by original data submitter

Sample

source_name
Input
cell line
breast cancer cell line MDA-MB-231
treatment
no treatment
chip antibody
none (input)

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
After cross-linking cells for 10 min with 1% formaldehyde and sonicating chromatin with a Diagenode Bioruptor, chromatin was immunoprecipitated using 5 µg of PRMT5 (Bethyl Labs, A300-849A) or 5 µg of rabbit serum for 1mg protein. ChIP-DNA was end repaired with T4 DNA polymerase and polynucleotide kinase. An A-base was added to the end-repaired DNA fragments. Solexa adaptors were ligated to the ChIP DNA fragments and 200-300bp size fractions were excised from 2% agarose gel stained with GelStar. Adaptor-modified fragments were enriched by 16 cycles of PCR amplification. The DNA library prep was validated in Bioanalyzer for quantity and size.

Sequencing Platform

instrument_model
Illumina Genome Analyzer

hg38

Number of total reads
77445052
Reads aligned (%)
97.9
Duplicates removed (%)
4.4
Number of peaks
5288 (qval < 1E-05)

hg19

Number of total reads
77445052
Reads aligned (%)
97.5
Duplicates removed (%)
5.3
Number of peaks
4834 (qval < 1E-05)

Base call quality data from DBCLS SRA