| Title: | Learning the kernel for rare variant genetic association test |
| Journal: | Frontiers in Genetics |
| Published: | 9 Oct 2023 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/37886683/ |
| DOI: | https://doi.org/10.3389/fgene.2023.1245238 |
| URL: | https://www.frontiersin.org/articles/10.3389/fgene.2023.1245238/pdf?isPublishedV2=False |
Publication 9402
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Abstract
Introduction: Compared to Genome-Wide Association Studies (GWAS) for common variants, single-marker association analysis for rare variants is underpowered. Set-based association analyses for rare variants are powerful tools that capture some of the missing heritability in trait association studies. Methods: We extend the convex-optimized SKAT (cSKAT) test set procedure which learns from data the optimal convex combination of kernels, to the full Generalised Linear Model (GLM) setting with arbitrary non-genetic covariates. We call this extended cSKAT (ecSKAT) and show that the resulting optimization problem is a quadratic programming problem that can be solved with no additional cost compared to cSKAT. Results: We show that a modified objective is related to an upper bound for the p-value through a decreasing exponential term in the objective function, indicating that optimizing this objective function is a principled way of learning the combination of kernels. We evaluate the performance of the proposed method on continuous and binary traits using simulation studies and illustrate its application using UK Biobank Whole Exome Sequencing data on hand grip strength and systemic lupus erythematosus rare variant association analysis. Discussion: Our proposed ecSKAT method enables correcting for important confounders in association studies such as age, sex or population structure for both quantitative and binary traits. Simulation studies showed that ecSKAT can recover sensible weights and achieve higher power across different sample sizes and misspecification settings. Compared to the burden test and SKAT method, ecSKAT gives a lower p-value for the genes tested in both quantitative and binary traits in the UKBiobank cohort.</p>
4 Authors
- Isak Falk
- Millie Zhao
- Juba Nait Saada
- Qi Guo
1 Application
| Application ID | Title |
|---|---|
| 43138 | Define disease endotypes agnostic of conventional diagnostic classes |
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