| Literature DB >> 33038041 |
Chloé Sarnowski1, Tianxiao Huan2,3, Deepti Jain4, Chunyu Liu1,2,3, Chen Yao2,3, Roby Joehanes2,3,5, Daniel Levy2,3, Josée Dupuis1.
Abstract
Multiple methods have been proposed to aggregate genetic variants in a gene or a region and jointly test their association with a trait of interest. However, these joint tests do not provide estimates of the individual effect of each variant. Moreover, few methods have evaluated the joint association of multiple variants with DNA methylation. We propose a method based on linear mixed models to estimate the joint and individual effect of multiple genetic variants on DNA methylation leveraging genomic annotations. Our approach is flexible, can incorporate covariates and annotation features, and takes into account relatedness and linkage disequilibrium (LD). Our method had correct Type-I error and overall high power for different simulated scenarios where we varied the number and specificity of functional annotations, number of causal and total genetic variants, frequency of genetic variants, LD, and genetic variant effect. Our method outperformed the family Sequence Kernel Association Test and had more stable estimations of effects than a classical single-variant linear mixed-effect model. Applied genome-wide to the Framingham Heart Study data, our method identified 921 DNA methylation sites influenced by at least one rare or low-frequency genetic variant located within 50 kilobases (kb) of the DNA methylation site.Entities:
Keywords: SNP-set; effect estimation; genomic annotation; multimarker test; single nucleotide polymorphisms
Mesh:
Year: 2020 PMID: 33038041 PMCID: PMC8005415 DOI: 10.1002/gepi.22369
Source DB: PubMed Journal: Genet Epidemiol ISSN: 0741-0395 Impact factor: 2.344