|
Status |
Public on Jul 09, 2019 |
Title |
chimp.iPSC.mTeSR1.HiC.Rep2 |
Sample type |
SRA |
|
|
Source name |
induced pluripotent stem cell
|
Organism |
Pan troglodytes |
Characteristics |
differentiation time: day00 cell type: chimp.iPSC
|
Growth protocol |
Chimpanzee and bonobo iPSCs were cultured on plates pre-coated with Matrigel (BD Biosciences) in commercial mTeSR1TM medium (Stemcell technology, 85850). Cells were passaged every 5-6 days with TrypLE (Life Technologies) at a split ratio of 1:10. ROCK inhibitor Y27632 (10uM) was added at least one hour prior to and 24 hours after passaging.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Briefly, 2 million cells were cross-linked with 1% formaldehyde for 10min at RT and reaction was quenched using 125 mM of Glycine for 5 min at RT. Nuclei were isolated and directly applied for digestion using 4 cutter restriction enzyme MboI (NEB) at 37 °C o/n. All libraries were constructed using standard illumina TruSeq LT library prep.
|
|
|
Library strategy |
Hi-C |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 4000 |
|
|
Description |
chimp.mt.hic on Series record
|
Data processing |
base-calling use bcl2fastq version 2.17 alignment was performed using bowtie2 for ATAC-seq, BWA for ChIP-seq and Hi-C, rnaSTAR for RNA-seq. Contacts for Hi-C data were stored in the juicer Hi-C format (could be opened with juicebox.jar provided by Aiden lab). Genome_build: hg19,calJac3, panPan2,panTro6 Supplementary_files_format_and_content: bigWig files for ChIP-seq and input, juicer hic format for Hi-C data and normalized read per million kilobases (RPKM) for RNA-seq.
|
|
|
Submission date |
Jun 28, 2019 |
Last update date |
Oct 22, 2024 |
Contact name |
Bing Ren |
E-mail(s) |
biren@ucsd.edu
|
Organization name |
University of California, San Diego
|
Street address |
9500 Gilman Drive
|
City |
La Jolla |
ZIP/Postal code |
92093 |
Country |
USA |
|
|
Platform ID |
GPL23423 |
Series (2) |
GSE116862 |
Chromatin structure dynamics during human cardiomyocyte differention reveals a role of HERV-H in demarcating TAD boundaries. |
GSE186958 |
Chromatin structure dynamics during human cardiomyocyte differention |
|
Relations |
BioSample |
SAMN12163260 |
SRA |
SRX6384259 |