ArticleBioinformatics (Oxford, England)2023
A maximum kernel-based association test to detect the pleiotropic genetic effects on multiple phenotypes.
Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Divided-and-combined association test for pleiotropic effects with GWAS summary statistics.BMC genomics · 2026Article
- The sequence kernel association test for the proportional odds model.Bioinformatics (Oxford, England) · 2025Article
- JASPER: Fast, powerful, multitrait association testing in structured samples gives insight on pleiotropy in gene expression.American journal of human genetics · 2024Article
- JASPER: fast, powerful, multitrait association testing in structured samples gives insight on pleiotropy in gene expression.bioRxiv : the preprint server for biology · 2023Article
- Pleiotropic genetic association analysis with multiple phenotypes using multivariate response best-subset selection.BMC genomics · 2023Article
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Authors and funding
3 authors.
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Abstract
motivationTesting the association between multiple phenotypes with a set of genetic variants simultaneously, rather than analyzing one trait at a time, is receiving increasing attention for its high statistical power and easy explanation on pleiotropic effects. The kernel-based association test (KAT), being free of data dimensions and structures, has proven to be a good alternative method for genetic association analysis with multiple phenotypes. However, KAT suffers from substantial power loss when multiple phenotypes have moderate to strong correlations. To handle this issue, we propose a maximum KAT (MaxKAT) and suggest using the generalized extreme value distribution to calculate its statistical significance under the null hypothesis.
resultsWe show that MaxKAT reduces computational intensity greatly while maintaining high accuracy. Extensive simulations demonstrate that MaxKAT can properly control type I error rates and obtain remarkably higher power than KAT under most of the considered scenarios. Application to a porcine dataset used in biomedical experiments of human disease further illustrates its practical utility. AVAILABILITY AND IMPLEMENTATION: The R package MaxKAT that implements the proposed method is available on Github https://github.com/WangJJ-xrk/MaxKAT.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.