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Sample GSM5363627 Query DataSets for GSM5363627
Status Public on Mar 15, 2022
Title 0d_HiC_replicate_3
Sample type SRA
 
Source name Liver
Organism Sus scrofa
Characteristics breed: Bama pig
tissue: Liver
condition: Developmental stage
age: the birth day
Sex: female
chip antibody: n/a
restriction enzyme: DpnII
Treatment protocol Six two-years-old female pigs were fed with a high fat diet (15.12 MJ·kg-1 metabolizable energy, 11.26% crude protein, 6.8% fat and 5% lysine) for 22 weeks, compared with the pigs of two-years-old fed with well-characterized normal diet for 22 weeks.
Extracted molecule genomic DNA
Extraction protocol Livers tissue was homogenized with liquid nitrogen then fixed with 4% formaldehyde solution and incubated at room temperature for 30 min. Glycine were added to a final concentration of 0.2 M to quench the fixing reaction, and incubated at room temperature for 5 min then centrifuge for 10 min at 1,000 g and 4˚C. Discarded supernatants and cells were lysed with 1M Tris-HCl, 1M NaCl, 10% CA-630 and protease inhibitors on ice for 15 min. Cell nucleus were washed twice and were permeabilized at 65˚C for 10 min with 1% SDS to a final concentration of 0.1%. To quench the SDS, added 10% TritonX-100 (0.1% final concentration) and incubated at 37˚C for 15 min. Then 200 U DpnII (a 4-cutter restriction enzyme) was added and digested chromatin at 37˚C for 90 min, 65˚C for 20 min and 25˚C for 5 min. The restriction fragment overhangs were filled and labelled by biotinylated nucleotides, then ligated in a small volume.
After crosslink reversal, ligated DNA was purified and sheared to a length of 300–500 bp, at which point ligation junctions were pulled down with magnetic beads and prepared for BGISEQ-500 sequencing.
 
Library strategy Hi-C
Library source genomic
Library selection other
Instrument model Illumina HiSeq 4000
 
Description 0d_3
all.samples.abindex.txt
0d.merged.replicates.tad.txt
developmental.consensus.TAD.txt
developmental.Dscore.txt
Data processing Reads were mapped to the pig genome (Sscrofa 11.1) by BWA (v 0.7.15).
Juicer were used HiC data processing to filter duplication, low-quality alignment read pairs (MAPQ < 30) as well as intra-fragment read pairs.
High-quality reads normalized with Knight-Ruiz [KR] algorithm and quantile algorithm to structure contact matrixes at 20 or 100 kb resolution.
Compartments A/B were identified with A-B index as described by M Jordan Rowley. et al. Mol Cell. 2017 (PMID: 28826674).
Locations of topologically associated domains (TADs) were computed by combining  directionality index (Dixon et al. Nature. 2012 [PMID: 22495300]) and insulation index (Emily Crane et al. Nature. 2017)
Genome_build: Sscrofa11.1
Supplementary_files_format_and_content: 20 and 100 kb matrixes, hic file
A-B index, txt file
locations of TAD for each sample, merged replicates, and consensus TAD,txt file
D-score, txt file
 
Submission date Jun 08, 2021
Last update date Mar 17, 2022
Contact name Jing Li
E-mail(s) lijing-jane@foxmail.com
Phone +8615882474902
Organization name Sichuan Agricultural University
Department College of Animal Science and Technology
Street address No. 211 Huimin Road, Wenjiang District
City Chengdu
State/province China
ZIP/Postal code 611130
Country China
 
Platform ID GPL22475
Series (1)
GSE176387 Three-dimensional geome study of procine livers during development and metabolic adaptation
Relations
BioSample SAMN18317842
SRA SRX10994528
SRA SRX10994529
SRA SRX10994530
SRA SRX10994531
SRA SRX10994532
SRA SRX10994533
SRA SRX10994534
SRA SRX10994535
SRA SRX10994536
SRA SRX10994537
SRA SRX10994538
SRA SRX10994539

Supplementary file Size Download File type/resource
GSM5363627_0d_3.TAD.txt.gz 21.0 Kb (ftp)(http) TXT
GSM5363627_0d_HiC_3.20k.100k.inter_30.hic 738.3 Mb (ftp)(http) HIC
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record
Processed data provided as supplementary file

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