Sample information curated by ChIP-Atlas

Antigen

Antigen Class
No description
Antigen
NA

Cell type

Cell type Class
Cardiovascular
Cell type
HMVEC
Primary Tissue
Blood Vessel
Tissue Diagnosis
Normal

Attributes by original data submitter

Sample

ENA first public
2015-05-22
ENA last update
2015-05-22
ENA-CHECKLIST
ERC000011
External Id
SAMEA3402916
INSDC center alias
CENTRE FOR CANCER BIOLOGY
INSDC center name
CENTRE FOR CANCER BIOLOGY
INSDC first public
2015-05-22T17:38:31Z
INSDC last update
2015-05-22T07:39:38Z
INSDC status
public
Submitter Id
1
cell line
Adult human dermal lymphatic microvascular endothelial cells HMVEC-dLyAd (hLEC)
cell type
Endothelial
common name
human
culture collection
Hematology department, Centre For Cancer Biology
geographic location (country and/or sea)
Australia
sample name
1
tissue lib
Lonza

Sequenced DNA Library

library_name
Illumina TruSeq
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
ChIP-Seq library preparation and sequencing was carried out at the ACRF Cancer Genomics Facility, Centre for Cancer Biology, Adelaide. ChIP-Seq libraries were prepared according to Illumina’s TruSeq Sample Prep Guide Revision A with some minor modifications.  Briefly, DNA was end-repaired, followed by adenylation of the 3’ ends.  Next, Illumina indexing adapters were ligated to the DNA. 18 cycles of PCR was performed to enrich for successfully adapter ligated molecules. Ligation products were purified with a 2% Pippin Prep gel (Sage Science), selecting a size range of 250 – 300 base pairs.  The size distribution and yield of the purified libraries were determined using an Agilent Bioanalyzer High Sensitivity chip and Qubit dsDNA HS assay (Invitrogen), respectively.  Libraries were pooled in equimolar ratios and sequenced in one lane of a HiSeq 2500 short read flowcell (1 x 50bp).

Sequencing Platform

instrument_model
Illumina HiSeq 2500

hg38

Number of total reads
35946092
Reads aligned (%)
97.9
Duplicates removed (%)
71.0
Number of peaks
8674 (qval < 1E-05)

hg19

Number of total reads
35946092
Reads aligned (%)
97.0
Duplicates removed (%)
72.5
Number of peaks
8671 (qval < 1E-05)

Base call quality data from DBCLS SRA