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- W3134225151 abstract "Induced pluripotent stem cells (iPSCs) are an established cellular system to study the impact of genetic variants in derived cell types and developmental contexts. However, in their pluripotent state, the disease impact of genetic variants is less well known. Here, we integrate data from 1,367 human iPSC lines to comprehensively map common and rare regulatory variants in human pluripotent cells. Using this population-scale resource, we report hundreds of new colocalization events for human traits specific to iPSCs, and find increased power to identify rare regulatory variants compared with somatic tissues. Finally, we demonstrate how iPSCs enable the identification of causal genes for rare diseases." @default.
- W3134225151 created "2021-03-15" @default.
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- W3134225151 date "2021-03-01" @default.
- W3134225151 modified "2023-10-18" @default.
- W3134225151 title "Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics" @default.
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- W3134225151 doi "https://doi.org/10.1038/s41588-021-00800-7" @default.
- W3134225151 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7944648" @default.
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