Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.

TitleRobust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.
Publication TypeJournal Article
Year of Publication2021
AuthorsKwong, AM, Blackwell, TW, LeFaive, J, de Andrade, M, Barnard, J, Barnes, KC, Blangero, J, Boerwinkle, E, Burchard, EG, Cade, BE, Chasman, DI, Chen, H, Conomos, MP, L Cupples, A, Ellinor, PT, Eng, C, Gao, Y, Guo, X, Irvin, MRyan, Kelly, TN, Kim, W, Kooperberg, C, Lubitz, SA, C Y Mak, A, Manichaikul, AW, Mathias, RA, Montasser, ME, Montgomery, CG, Musani, S, Palmer, ND, Peloso, GM, Qiao, D, Reiner, AP, Roden, DM, M Shoemaker, B, Smith, JA, Smith, NL, Su, JLasky, Tiwari, HK, Weeks, DE, Weiss, ST, Scott, LJ, Smith, AV, Abecasis, GR, Boehnke, M, Kang, HMin
Corporate AuthorsNHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Analysis Working Group
JournalGenetics
Volume218
Issue1
Date Published2021 May 17
ISSN1943-2631
KeywordsAlleles, Gene Frequency, Genetics, Population, Genotype, Humans, Linkage Disequilibrium, Models, Genetic, Models, Statistical, Phenotype, Software
Abstract

Traditional Hardy-Weinberg equilibrium (HWE) tests (the χ2 test and the exact test) have long been used as a metric for evaluating genotype quality, as technical artifacts leading to incorrect genotype calls often can be identified as deviations from HWE. However, in data sets composed of individuals from diverse ancestries, HWE can be violated even without genotyping error, complicating the use of HWE testing to assess genotype data quality. In this manuscript, we present the Robust Unified Test for HWE (RUTH) to test for HWE while accounting for population structure and genotype uncertainty, and to evaluate the impact of population heterogeneity and genotype uncertainty on the standard HWE tests and alternative methods using simulated and real sequence data sets. Our results demonstrate that ignoring population structure or genotype uncertainty in HWE tests can inflate false-positive rates by many orders of magnitude. Our evaluations demonstrate different tradeoffs between false positives and statistical power across the methods, with RUTH consistently among the best across all evaluations. RUTH is implemented as a practical and scalable software tool to rapidly perform HWE tests across millions of markers and hundreds of thousands of individuals while supporting standard VCF/BCF formats. RUTH is publicly available at https://www.github.com/statgen/ruth.

DOI10.1093/genetics/iyab044
Alternate JournalGenetics
PubMed ID33720349
PubMed Central IDPMC8128395
Grant ListU54 GM104938 / GM / NIGMS NIH HHS / United States
R01 HL120393 / HL / NHLBI NIH HHS / United States
U01 HL120393 / HL / NHLBI NIH HHS / United States
U01 MH105653 / MH / NIMH NIH HHS / United States
HHSN268201800001C / HL / NHLBI NIH HHS / United States
K01 HL129039 / HL / NHLBI NIH HHS / United States
R01 DA037904 / DA / NIDA NIH HHS / United States
R01 HL117626 / HL / NHLBI NIH HHS / United States
K01 HL135405 / HL / NHLBI NIH HHS / United States
R01 HL142711 / HL / NHLBI NIH HHS / United States
R01 HL113326 / HL / NHLBI NIH HHS / United States
P01 HL045522 / HL / NHLBI NIH HHS / United States
R01 AI132476 / AI / NIAID NIH HHS / United States
R01 HG009976 / HG / NHGRI NIH HHS / United States
P30 DK020572 / DK / NIDDK NIH HHS / United States
R03 HL154284 / HL / NHLBI NIH HHS / United States
U01 HL137182 / HL / NHLBI NIH HHS / United States
R01 HG007022 / HG / NHGRI NIH HHS / United States
U01 CA182913 / CA / NCI NIH HHS / United States
U01 HL117626 / HL / NHLBI NIH HHS / United States

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