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General retrospective mega‐analysis framework for rare variant association tests
Author(s) -
Chien LiChu,
Chiu YenFeng
Publication year - 2018
Publication title -
genetic epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.301
H-Index - 98
eISSN - 1098-2272
pISSN - 0741-0395
DOI - 10.1002/gepi.22147
Subject(s) - categorical variable , genetic association , population stratification , population , sample size determination , statistics , covariate , econometrics , genetics , biology , medicine , mathematics , genotype , gene , environmental health , single nucleotide polymorphism
Here, we describe a retrospective mega‐analysis framework for gene‐ or region‐based multimarker rare variant association tests. Our proposed mega‐analysis association tests allow investigators to combine longitudinal and cross‐sectional family‐ and/or population‐based studies. This framework can be applied to a continuous, categorical, or survival trait. In addition to autosomal variants, the tests can be applied to conduct mega‐analyses on X‐chromosome variants. Tests were built on study‐specific region‐ or gene‐level quasiscore statistics and, therefore, do not require estimates of effects of individual rare variants. We used the generalized estimating equation approach to account for complex multiple correlation structures between family members, repeated measurements, and genetic markers. While accounting for multilevel correlations and heterogeneity across studies, the test statistics were computationally efficient and feasible for large‐scale sequencing studies. The retrospective aspect of association tests helps alleviate bias due to phenotype‐related sampling and type I errors due to misspecification of phenotypic distribution. We evaluated our developed mega‐analysis methods through comprehensive simulations with varying sample sizes, covariates, population stratification structures, and study designs across multiple studies. To illustrate application of the proposed framework, we conducted a mega‐association analysis combining a longitudinal family study and a cross‐sectional case–control study from Genetic Analysis Workshop 19.