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Experiment information
Accession CRX791070
Organism Brassica rapa var. purpuraria
Title HongShanCaiTai HiC
BioProject PRJCA019480
BioSample SAMC3057464
Platform Illumina NovaSeq 6000
Library
Library name Construction protocol Strategy Source Selection Layout
the plant materials were fixed in NIB buffer and then lysed by 1.0% of SDS in Triton X-100. The DNA in the nuclei was digested by endonuclease DpnII (NEB). The blunt ends of digested DNA were labelled by Biotin-14-dATP (TriLINK Biotechnologies, USA). Then the samples were deproteinized with proteinase K (Thermo Fisher Scientific, USA) and purified using QIAamp DNA Mini Kit (Qiagen, USA) Hi-C GENOMIC PCR PAIRED
Processing Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
Release date2024-03-29
Run
Run accession Run data file information
File nameFile size (MB)
CRR875505 CRR875505_f1.fq.gz
CRR875505_r2.fq.gz
24,679.88
25,074.72
SubmitterYifan Zhou (117711731@qq.com)
OrganizationWuhan University
Date submitted2023-09-12