Evidence map›Paper›PMID 36279152›Full record

ArticleThe international journal of biostatistics2023

A copula-based set-variant association test for bivariate continuous, binary or mixed phenotypes.

Julien St-Pierre, Karim Oualkacha

Abstract read
In one paragraph

Article in The international journal of biostatistics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Julien St-PierreDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, QC, Canada.ORCID 0000-0001-9627-576X
Karim OualkachaDépartement de Mathématiques, Université du Québec à Montréal, Montreal, QC, Canada.ORCID 0000-0002-9911-079X

Funding

Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009Wellcome TrustWellcome Trust WT091310
6 · The paper itself

Abstract

In genome wide association studies (GWAS), researchers are often dealing with dichotomous and non-normally distributed traits, or a mixture of discrete-continuous traits. However, most of the current region-based methods rely on multivariate linear mixed models (mvLMMs) and assume a multivariate normal distribution for the phenotypes of interest. Hence, these methods are not applicable to disease or non-normally distributed traits. Therefore, there is a need to develop unified and flexible methods to study association between a set of (possibly rare) genetic variants and non-normal multivariate phenotypes. Copulas are multivariate distribution functions with uniform margins on the [0, 1] interval and they provide suitable models to deal with non-normality of errors in multivariate association studies. We propose a novel unified and flexible copula-based multivariate association test (CBMAT) for discovering association between a genetic region and a bivariate continuous, binary or mixed phenotype. We also derive a data-driven analytic

Indexed as

Genome-Wide Association StudyModels, GeneticComputer SimulationHumansLinear ModelsPhenotypecopulasgene-based testsgeneralized linear mixed modelsmixed binary-continuous phenotypesstatistical geneticsvariance component score test

Identifiers

PMID36279152
PMCPMC10644254

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.