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Status |
Public on Jul 04, 2024 |
Title |
U2OS_siCtrl_HiC_rep1 |
Sample type |
SRA |
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Source name |
U2OS cells
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Organism |
Homo sapiens |
Characteristics |
cell type: U2OS cells genotype: control treatment: untreated
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Extracted molecule |
genomic DNA |
Extraction protocol |
The cross-linked cells were lysed in lysis buffer,fragmentation of the genome using restriction enzymes Hi-C libraries were prepared for sequencing using standard Illumina protocols
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Library strategy |
Hi-C |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 4000 |
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Data processing |
Raw sequencing data was first filtered by Trimmomatic (version: 0.36), low-quality reads were discarded and adaptor sequences were trimmed The BWA package was used to map the sequences against the human reference genome with the parameter -n 0. Mapped reads with MAPQ quality scores ≥20 were chosen for further analysis. We applied the ICE method to normalize the interaction matrix for different resolutions If a region between two adjacent boundaries was less than 400 kb, the region was marked as a TAD boundary The Juicer pipeline’s HiCCUPS was applied for discovery of locally enriched peaks Genome_build: hg19 Supplementary_files_format_and_content: all the locally enriched peaks were determined by HiCCUPS
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Submission date |
Jul 04, 2021 |
Last update date |
Jul 04, 2024 |
Contact name |
wenhui Zhao |
E-mail(s) |
ZHAOWENHUI@CQU.EDU.CN
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Organization name |
Peking University
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Street address |
5 Yiheyuan Road, Haidian District
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City |
Beijing |
ZIP/Postal code |
100871 |
Country |
China |
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Platform ID |
GPL20301 |
Series (1) |
GSE179410 |
NAT10-mediated β-hydroxybutyrylation Rewires Genomic 3D Conformation and Replication Timing [Hi-C] |
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Relations |
BioSample |
SAMN20056915 |
SRA |
SRX11348961 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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