Sample information curated by ChIP-Atlas

Antigen

Antigen Class
ATAC-Seq
Antigen
ATAC-Seq

Cell type

Cell type Class
Cardiovascular
Cell type
Aortic valve interstitial cells
NA
NA

Attributes by original data submitter

Sample

source_name
Human aortic valve interstitial cells from non-mineralized aortic valves
cell type
aortic valve interstitial cells

Sequenced DNA Library

library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Human aortic valve interstitial cells were isolated from control non-mineralized aortic valves obtained from patients undergoing heart transplantation. The protocol was approved by the local ethical committee and informed consent was obtained from the subjects. Aortic leaflets were cut into pieces and incubated in 0.3% type I collagenase (Invitrogen, Thermo Fisher Scientific, ON, Canada) at 37°C for 45 minutes, then filtered through a 70 µm mesh, centrifuged for 5 minutes at 1,500 rpm and resuspended in complete media (DMEM, 10% FBS with L-glutamine and sodium pyruvate). Cells were used between passages 3 to 7. Nuclei from approximatively 2.5-4 x 105 cells were prepared as previously described (Shashikant T, et al. 2018, BMC Genomics). Libraries were first amplified for 5 cycles using custom-synthesized index primers and then a second amplification was performed. The appropriate number of additional PCR cycles was determined using quantitative real-time PCR by plotting the Rn value (fluorescent signal from SYBR Green I) versus cycle number and determining the cycle number corresponding to one-third of the maximum fluorescent intensity. Libraries were PCR-amplified for 4-7 cycles. After PCR amplification, libraries were purified using DNA clean up & concentrator kit (Zymo Research, Cedarlane, Canada)Library quality was assessed on a BioAnalyser (Agilent, ON, Canada) using Agilent High Sensitivity DNA kit (Agilent, ON, Canada). Sequencing was performed on an Illumina HiSeq4000 (UCSD IGM Genomics Facility, CA, USA).

Sequencing Platform

instrument_model
Illumina HiSeq 4000

hg38

Number of total reads
56520355
Reads aligned (%)
63.7
Duplicates removed (%)
68.4
Number of peaks
5379 (qval < 1E-05)

hg19

Number of total reads
56520355
Reads aligned (%)
63.4
Duplicates removed (%)
68.8
Number of peaks
5293 (qval < 1E-05)

Base call quality data from DBCLS SRA