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BRASS: Permutation methods for binary traits in genetic association studies with structured samples.
Mbatchou, Joelle; Abney, Mark; McPeek, Mary Sara.
Afiliação
  • Mbatchou J; Regeneron Genetics Center, Tarrytown, New York, United States of America.
  • Abney M; Department of Statistics, The University of Chicago, Chicago, Illinois, United States of America.
  • McPeek MS; Department of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
PLoS Genet ; 19(11): e1011020, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37934792
ABSTRACT
In genetic association analysis of complex traits, permutation testing can be a valuable tool for assessing significance when the distribution of the test statistic is unknown or not well-approximated. This commonly arises, e.g, in tests of gene-set, pathway or genome-wide significance, or when the statistic is formed by machine learning or data adaptive methods. Existing applications include eQTL mapping, association testing with rare variants, inclusion of admixed individuals in genetic association analysis, and epistasis detection among many others. For genetic association testing in samples with population structure and/or relatedness, use of naive permutation can lead to inflated type 1 error. To address this in quantitative traits, the MVNpermute method was developed. However, for association mapping of a binary trait, the relationship between the mean and variance makes both naive permutation and the MVNpermute method invalid. We propose BRASS, a permutation method for binary traits, for use in association mapping in structured samples. In addition to modeling structure in the sample, BRASS allows for covariates, ascertainment and simultaneous testing of multiple markers, and it accommodates a wide range of test statistics. In simulation studies, we compare BRASS to other permutation and resampling-based methods in a range of scenarios that include population structure, familial relatedness, ascertainment and phenotype model misspecification. In these settings, we demonstrate the superior control of type 1 error by BRASS compared to the other 6 methods considered. We apply BRASS to assess genome-wide significance for association analyses in domestic dog for elbow dysplasia (ED) and idiopathic epilepsy (IE). For both traits we detect previously identified associations, and in addition, for ED, we detect significant association with a SNP on chromosome 35 that was not detected by previous analyses, demonstrating the potential of the method.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Modelos Genéticos Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Modelos Genéticos Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article