UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test
Author:
Funder
National Institutes of Health
NIH
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank;Van Hout;bioRxiv,2019
2. The UK Biobank resource with deep phenotyping and genomic data;Bycroft;Nature,2018
3. Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study;Dewey;Science,2016
4. Unravelling the human genome-phenome relationship using phenome-wide association studies;Bush;Nat. Rev. Genet.,2016
5. A fast and accurate algorithm to test for binary phenotypes and its application to PheWAS;Dey;Am. J. Hum. Genet.,2017
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