ArticleBehavior genetics2018
Adaptive SNP-Set Association Testing in Generalized Linear Mixed Models with Application to Family Studies.
Article in Behavior genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- A gene-level methylome-wide association analysis identifies novel Alzheimer's disease genes.Bioinformatics (Oxford, England) · 2021Article
- Modeling the Dependence Structure in Genome Wide Association Studies of Binary Phenotypes in Family Data.Behavior genetics · 2020Article
- Two-phase SSU and SKAT in genetic association studies.Journal of genetics · 2020Article
- Data-adaptive multi-locus association testing in subjects with arbitrary genealogical relationships.Statistical applications in genetics and molecular biology · 2019Article
- Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies.American journal of human genetics · 2019Article
- An adaptive gene-level association test for pedigree data.BMC genetics · 2018Article
- Methods and results from the genome-wide association group at GAW20.BMC genetics · 2018Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
In genome-wide association studies (GWAS), it has been increasingly recognized that, as a complementary approach to standard single SNP analyses, it may be beneficial to analyze a group of functionally related SNPs together. Among the existent population-based SNP-set association tests, two adaptive tests, the aSPU test and the aSPUpath test, offer a powerful and general approach at the gene- and pathway-levels by data-adaptively combining the results across multiple SNPs (and genes) such that high statistical power can be maintained across a wide range of scenarios. We extend the aSPU and the aSPUpath test to familial data under the framework of the generalized linear mixed models (GLMMs), which can take account of both subject relatedness and possible population structure. As in population-based GWAS, the proposed aSPU and aSPUpath tests require only fitting a single and common GLMM (under the null hypothesis) for all the SNPs, thus are computationally efficient and feasible for large GWAS data. We illustrate our approaches in identifying genes and pathways associated with alcohol dependence in the Minnesota Twin Family Study. The aSPU test detected a gene associated with the trait, in contrast to none by the standard single SNP analysis. Our aSPU test also controlled Type I errors satisfactorily in a small simulation study. We provide R code to conduct the aSPU and aSPUpath tests for familial and other correlated data.
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Registered trials
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