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Experiment information
Accession CRX470394
Organism Lycium barbarum
Title Hi-C
BioProject PRJCA010231
BioSample SAMC810313
Platform Illumina HiSeq X Ten
Library
Library name Construction protocol Strategy Source Selection Layout
Two Hi-C libraries were performed as described by Chang Liu (2017) except for a few changes. Briefly in three steps, fresh tender leaves were fixed with 1% (v/v) formaldehyde and then nuclei isolated, Cross linking DNA was digested with MboI, Sticky overhangs were filled in with biotin-14-dCTP (Invitrogen, 19518018), blunt ends were ligated and proximity fragment formed chimeric junctions. Purified DNA was sheared to 200bp-500bp by Covaris S2. Chimeric fragments of biotin-labeled were captured through dynabeads streptavidin C1, which were created DNA library using NEBNext Ultra II DNA enzyme and corresponding adapters. Hi-C GENOMIC RANDOM PAIRED
Processing Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
Release date2024-10-12
Run
Run accession Run data file information
File nameFile size (MB)
CRR530530 CRR530530_f1.fq.gz
CRR530530_r2.fq.gz
40,623.93
42,287.8
CRR530531 CRR530531_f1.fq.gz
CRR530531_r2.fq.gz
40,962.81
45,500.3
SubmitterHaiyan Yue (yue_yhy@ibp.ac.cn)
OrganizationInstitute of Biophysics, Chinese Academy of Sciences
Date submitted2022-07-11
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