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Sample GSM5417201 Query DataSets for GSM5417201
Status Public on Jul 04, 2024
Title U2OS_siCtrl_HiC_rep1
Sample type SRA
 
Source name U2OS cells
Organism Homo sapiens
Characteristics cell type: U2OS cells
genotype: control
treatment: untreated
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
 
Library strategy Hi-C
Library source genomic
Library selection other
Instrument model Illumina HiSeq 4000
 
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
 
Submission date Jul 04, 2021
Last update date Jul 04, 2024
Contact name wenhui Zhao
E-mail(s) ZHAOWENHUI@CQU.EDU.CN
Organization name Peking University
Street address 5 Yiheyuan Road, Haidian District
City Beijing
ZIP/Postal code 100871
Country China
 
Platform ID GPL20301
Series (1)
GSE179410 NAT10-mediated β-hydroxybutyrylation  Rewires Genomic 3D Conformation and Replication Timing [Hi-C]
Relations
BioSample SAMN20056915
SRA SRX11348961

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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