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Status |
Public on Apr 30, 2022 |
Title |
Dissecting genetic components associated with eye disease using integrative genomic analysis [Capture HiC] |
Organism |
Homo sapiens |
Experiment type |
Other
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Summary |
GWAS studies have revealed thousands of variants strongly associated with AMD, yet connecting these variants to their cognate genes has not been explored. In this study we fine-mapped AMD risk loci and examined long-range cis chromatin interactions at essential genes of RPE function and disease-associated variants in iPSC-induced retinal pigmented epithelium (RPE) and primary RPE.
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Overall design |
Capture HiC from iPSCs (2 replicates), iPSC-induced RPE (2 replicates).
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Contributor(s) |
Jamieson K, Shen Y |
Citation missing |
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Submission date |
Apr 27, 2022 |
Last update date |
Apr 30, 2022 |
Contact name |
Kirsty Jamieson |
E-mail(s) |
kirstyjamieson@gmail.com
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Organization name |
University of California
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Street address |
400 Parnassus Ave
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City |
San Francisco |
ZIP/Postal code |
94143 |
Country |
USA |
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Platforms (1) |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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Samples (4)
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GSM6069388 |
Capture HiC, iPSC-induced RPE, biol rep1 |
GSM6069389 |
Capture HiC, iPSC-induced RPE, biol rep2 |
GSM6069390 |
Capture HiC, primary RPE, biol rep1 |
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This SubSeries is part of SuperSeries: |
GSE201681 |
Dissecting genetic components associated with eye disease using integrative genomic analysis |
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Relations |
BioProject |
PRJNA832670 |