Evidence map›Paper›PMID 37104737›Full record

ArticleBioinformatics (Oxford, England)2023

A maximum kernel-based association test to detect the pleiotropic genetic effects on multiple phenotypes.

Jinjuan Wang, Mingya Long, Qizhai Li

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jinjuan WangSchool of Mathematics and Statistics, Beijing Institute of Technology, Beijing 100081, China.ORCID 0000-0002-4320-8528
Mingya LongLSC Academy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing 100190, China.
Qizhai LiLSC Academy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing 100190, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Genome-Wide Association StudyModels, GeneticAnimalsComputer SimulationHumansPhenotypeSwine

Identifiers

PMID37104737
PMCPMC10174706

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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.