Sample information curated by ChIP-Atlas

Antigen

Antigen Class
No description
Antigen
NA

Cell type

Cell type Class
Breast
Cell type
CAL-51
Primary Tissue
Breast
Site of Extraction
Pleura
Tissue Diagnosis
Adenocarcinoma

Attributes by original data submitter

Sample

ENA first public
2017-05-17
ENA last update
2016-11-04
ENA-CHECKLIST
ERC000011
External Id
SAMEA4534849
INSDC center alias
LabMedMolGe Unisa Department of Medicine and Surgery University of Salerno
INSDC center name
LabMedMolGe Unisa Department of Medicine and Surgery University of Salerno
INSDC first public
2017-05-17T17:02:12Z
INSDC last update
2016-11-04T13:49:16Z
INSDC status
public
Submitter Id
E-MTAB-5217:Sample 2
broker name
ArrayExpress
cell line
CAL51
common name
human
sample name
E-MTAB-5217:Sample 2

Sequenced DNA Library

library_name
Sample 2_s
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
CAL51 cells were cultured in DMEM/F12 complemented with 10% FBS for 48h. Chromatin was immunoprecipitated from three technical replicates using an ChIP-grade anti-YAP antibody (Cell Signaling Technologies) and following the manufacture’s instructions (PierceAgarose ChIP Kit, Thermo Fisher Scientific). Control ChIP was performed by using input DNA. Library preparation and sequencing was performed by Genomix4Life S.r.l (Baronissi, Italy). Size distribution of each ChIP DNA sample was assessed by running a 1μl aliquot on Agilent High Sensitivity DNA chip using an Agilent Technologies 2100 Bioanalyzer (Agilent Technologies). The concentration of each DNA sample was determined by using Quant-IT DNA Assay Kit- High Sensitivity and a Qubit Fluorometer (Life Technologies). 10 ng of purified ChIP DNA were used as starting material for sequencing libraries preparation.

Sequencing Platform

instrument_model
Illumina HiSeq 2500

hg38

Number of total reads
53846935
Reads aligned (%)
85.0
Duplicates removed (%)
8.4
Number of peaks
1009 (qval < 1E-05)

hg19

Number of total reads
53846935
Reads aligned (%)
84.2
Duplicates removed (%)
9.3
Number of peaks
1062 (qval < 1E-05)

Base call quality data from DBCLS SRA