Evidence map›Paper›PMID 35482827›Full record

ArticlePloS one2022

A computationally efficient clustering linear combination approach to jointly analyze multiple phenotypes for GWAS.

Meida Wang, Shuanglin Zhang, Qiuying Sha

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Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Meida WangMathematical Sciences, Michigan Technological University, Houghton, MI, United States of America.
Shuanglin ZhangMathematical Sciences, Michigan Technological University, Houghton, MI, United States of America.ORCID 0000-0002-9478-1199
Qiuying ShaMathematical Sciences, Michigan Technological University, Houghton, MI, United States of America.ORCID 0000-0002-9342-3269

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There has been an increasing interest in joint analysis of multiple phenotypes in genome-wide association studies (GWAS) because jointly analyzing multiple phenotypes may increase statistical power to detect genetic variants associated with complex diseases or traits. Recently, many statistical methods have been developed for joint analysis of multiple phenotypes in genetic association studies, including the Clustering Linear Combination (CLC) method. The CLC method works particularly well with phenotypes that have natural groupings, but due to the unknown number of clusters for a given data, the final test statistic of CLC method is the minimum p-value among all p-values of the CLC test statistics obtained from each possible number of clusters. Therefore, a simulation procedure needs to be used to evaluate the p-value of the final test statistic. This makes the CLC method computationally demanding. We develop a new method called computationally efficient CLC (ceCLC) to test the association between multiple phenotypes and a genetic variant. Instead of using the minimum p-value as the test statistic in the CLC method, ceCLC uses the Cauchy combination test to combine all p-values of the CLC test statistics obtained from each possible number of clusters. The test statistic of ceCLC approximately follows a standard Cauchy distribution, so the p-value can be obtained from the cumulative density function without the need for the simulation procedure. Through extensive simulation studies and application on the COPDGene data, the results demonstrate that the type I error rates of ceCLC are effectively controlled in different simulation settings and ceCLC either outperforms all other methods or has statistical power that is very close to the most powerful method with which it has been compared.

Indexed as

Genome-Wide Association StudyCluster AnalysisComputer SimulationGenetic Association StudiesPhenotype

Identifiers

PMID35482827
PMCPMC9049312

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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.