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Status |
Public on Sep 01, 2015 |
Title |
Hi-C, SK-N-SH, Replicate 1 |
Sample type |
SRA |
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Source name |
SK-N-SH
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Organism |
Homo sapiens |
Characteristics |
cell line: SK-N-SH
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Treatment protocol |
Cells crosslinked for 10 minutes at room temperature with 1% formadehyde. Quencing was performed with 0.125M glycine for 5 minutes are room temperature
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Growth protocol |
Cells cultured in RPMI media supplemented with 10% FBS
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Extracted molecule |
genomic DNA |
Extraction protocol |
Hi-C and library prep were performed as previously described (Dixon et al., Nature. 2012. PMID:22495300).
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Library strategy |
OTHER |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 2500 |
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Data processing |
Hi-C reads were mapped to hg19 using BWA-MEM. Reads were aligned as single ends, and read pairs are then re-constructed after mapping. Unmapped reads were filtered out and PCR duplicate reads were removed with PicardTools MarkDuplicates. Contact matrices were constructed at 40kb resolution and normalized with HiCNorm (Hu, M. et al., Bioinformatics. 2012. PMID: 23023982). Topologically associated domains (“TADs”) were identified based on Directionality Index (“DI”) as described previously (Dixon et al., Nature. 2012. PMID: 22495300), with one exception: DI was calculated using a sliding window of 300 kb upstream/downstream of the view point. Genome_build: hg19
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Submission date |
Jul 18, 2015 |
Last update date |
May 15, 2019 |
Contact name |
David Gorkin |
E-mail(s) |
dgorkin@ucsd.edu
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Organization name |
Ludwig Institute for Cancer Research
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Lab |
Bing Ren
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Street address |
9500 Gilman Dr. CMM-East 2071
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City |
La Jolla |
State/province |
California |
ZIP/Postal code |
92093 |
Country |
USA |
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Platform ID |
GPL16791 |
Series (1) |
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Relations |
BioSample |
SAMN03879914 |
SRA |
SRX1100381 |
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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