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Experiment information
Accession CRX912987
Organism Monochamus alternatus
Title Mal_Hi-C
BioProject PRJCA022378
BioSample SAMC3281316
Platform DNBSEQ-T7
Library
Library name Construction protocol Strategy Source Selection Layout
The tissue was vacuum infiltrated in nuclei isolation buffer supplemented with 2% formaldehyde. Adding glycine and additional vacuum infiltration to stop the crosslinking. Fixed tissue was grounded to powder and re-suspended in nuclei isolation buffer. The purified nuclei were digested with 100units of DpnII and marked by incubating with biotin-14-dATP. Removed biotin-14-dATP from non-ligated DNA ends using T4 DNA polymerase. The ligated DNA was sheared into 300-600 bp fragments, and then was blunt-end repaired and A-tailed, followed by purification through biotin-streptavidin-mediated pull down. Hi-C GENOMIC other PAIRED
Processing Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
Release date2024-03-21
Run
Run accession Run data file information
File nameFile size (MB)
CRR1002984 CRR1002984_f1.fq.gz
CRR1002984_r2.fq.gz
53,122.34
50,890.63
SubmitterDunyang Yu (yukun7879@126.com)
OrganizationAgricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences
Date submitted2023-12-28
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Experiments(2)