Evidence map›Paper›PMID 42114112›Full record

ArticleGenetics2026

Kernel-smoothed permutation for extreme P-value estimation in genetic association studies.

Jiayi Bian, Jingjing Wu, M Ethan MacDonald, Lang Wu, Quan Long, Caifeng Li

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jiayi BianDepartment of Mathematics and Statistics, University of Calgary, Calgary, Alberta T2N 1N4, Canada.ORCID 0009-0001-8873-4839
Jingjing WuDepartment of Mathematics and Statistics, University of Calgary, Calgary, Alberta T2N 1N4, Canada.ORCID 0000-0003-4555-1490
M Ethan MacDonaldDepartment of Electrical and Software Engineering, University of Calgary, Calgary, Alberta T2N 1N4, Canada.ORCID 0000-0001-5421-3536
Lang WuDepartment of Interdisciplinary Oncology and Department of Genetics, LSU-LCMC Health Cancer Center, School of Medicine, Louisiana State University Health Sciences Center, Louisiana State University, New Orleans, LA 70112, United States.ORCID 0000-0001-9938-3627
Quan LongDepartment of Mathematics and Statistics, University of Calgary, Calgary, Alberta T2N 1N4, Canada.ORCID 0000-0003-3795-1873
Caifeng LiDepartment of Mathematics and Statistics, University of Calgary, Calgary, Alberta T2N 1N4, Canada.ORCID 0000-0001-9157-367X

Funding

Alberta Innovates Graduate Student ScholarshipsAlberta Innovates LevMax-Health Program Bridge 222300769Canada Foundation for Innovation 36605Cumming School of Medicine Graduate ScholarshipNew Frontiers in Research NFRFE-2023-00291NSERC Discovery RGPIN-2024-04679NSERC Discovery RGPIN-2024-06154
6 · The paper itself

Abstract

In genetic association studies, permutation tests serve as a cornerstone to estimate P-values. This is because researchers may design new test statistics without a known closed-form distribution, or the assumption of a well-established test may not hold. However, permutation tests require a vast number of permutations, which is proportional to the magnitude of the actual P-values. When it comes to genome-wide association studies where multiple-test corrections are routinely conducted, the actual P-values are extremely small, requiring a daunting number of permutations that may be beyond the available computational resources. Existing models that reduce the required number of permutations all assume a specific format of the test statistic to exploit its specific statistical properties. We propose Kernel-smoothed permutation, which is a model-free method universally applicable to any statistic. Our tool forms the null distribution of test statistics using a kurtosis-driven transformation, followed by a kernel-based density estimation. We compared our Kernel-smoothed permutation to Naïve permutation using statistics from known closed-form null distributions. Based on 3 frequently used test statistics in association studies, ie t-test, sequence kernel association test, and chi-squared test, we demonstrated that our model reduced the required number of permutations by a magnitude with similar or higher accuracy. Based on a real-world genome-wide association study analysis, we used Crohn's disease cohort to further confirm that our model substantially outperforms the Naïve permutation.

Indexed as

Genetic Association StudiesGenome-Wide Association StudyModels, GeneticModels, StatisticalAlgorithmsComputer SimulationHumansPolymorphism, Single Nucleotidegenetic association studieskernel-based density estimationpermutation testP-value estimationtest statistic

Identifiers

PMID42114112
PMCPMC13334087

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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.