ArticleBiostatistics (Oxford, England)2022
An optimal kernel-based multivariate U-statistic to test for associations with multiple phenotypes.
Article in Biostatistics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Robust multivariate regression controlling false discoveries for microbiome data.Bioinformatics (Oxford, England) · 2025Article
- Pleiotropic genetic association analysis with multiple phenotypes using multivariate response best-subset selection.BMC genomics · 2023Article
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Authors and funding
2 authors.
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Abstract
Set-based analysis that jointly considers multiple predictors in a group has been broadly conducted for association tests. However, their power can be sensitive to the distribution of phenotypes, and the underlying relationships between predictors and outcomes. Moreover, most of the set-based methods are designed for single-trait analysis, making it hard to explore the pleiotropic effect and borrow information when multiple phenotypes are available. Here, we propose a kernel-based multivariate U-statistics (KMU) that is robust and powerful in testing the association between a set of predictors and multiple outcomes. We employed a rank-based kernel function for the outcomes, which makes our method robust to various outcome distributions. Rather than selecting a single kernel, our test statistics is built based on multiple kernels selected in a data-driven manner, and thus is capable of capturing various complex relationships between predictors and outcomes. The asymptotic properties of our test statistics have been developed. Through simulations, we have demonstrated that KMU has controlled type I error and higher power than its counterparts. We further showed its practical utility by analyzing a whole genome sequencing data from Alzheimer's Disease Neuroimaging Initiative study, where novel genes have been detected to be associated with imaging phenotypes.
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