Evidence map›Paper›PMID 42241225›Full record

ArticleBioinformatics (Oxford, England)2026

Evaluation of epistasis detection methods for quantitative phenotypes.

Stanislav Listopad, Gauri Renjith, Qian Peng

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Article in Bioinformatics (Oxford, England), 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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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Stanislav ListopadDepartment of Neuroscience, The Scripps Research Institute, La Jolla, CA 92037, United States.ORCID 0000-0002-7983-7879
Gauri RenjithDepartment of Computer Science and Engineering, University of California, San Diego, CA 92093, United States.
Qian PengDepartment of Neuroscience, The Scripps Research Institute, La Jolla, CA 92037, United States.

Funding

Neurpsychopharmacology-Multidisciplinary TrainingT32AA007456 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI MARISA ROBERTO · 1985 to 2026
$13.4M
Identifying specific genetic pathway interactions for drug use and abuse through integrative omicsDP1DA054373 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI PENG, QIAN · 2021 to 2025
$2.7M
National Institute on Alcohol Abuse and Alcoholism (NIAAA) National Institute on Drug Abuse (NIDA)National Institutes of Health (NIH)NIAAA and NIDANIAAA NIH HHS T32 AA007456NIDA NIH HHS DP1 DA054373
6 · The paper itself

Abstract

motivationEpistasis, or genetic interaction, plays a crucial role in shaping complex traits and has been increasingly recognized for its widespread influence in genetic architectures. While epistasis detection has been extensively evaluated in case-control studies, its performance with quantitative phenotypes remains comparatively understudied.

resultsWe identified and evaluated six epistasis detection methods applicable to quantitative trait analysis: EpiSNP, Matrix Epistasis, MIDESP, PLINK Epistasis, QMDR, and REMMA. Using the EpiGEN simulator, we generated synthetic datasets modeling four classes of pairwise SNP interactions-dominant, multiplicative, recessive, and XOR. We also assessed BOOST and MDR algorithms using discretized (case-control) versions of the same datasets. Performance varied notably by interaction type: REMMA achieved the highest overall detection rate (55%), particularly excelling with dominant interactions (100%). MDR excelled with multiplicative (57%) and XOR (69%) interactions. Meanwhile, EpiSNP attained the best performance for recessive interactions (67%). All methods except BOOST produced F1 scores below 0.05 for most interaction types. We further evaluated the methods using a real-world dataset. When applied to the Adolescent Brain Cognitive Development dataset to analyse the externalizing behavior phenotype, both PLINK Epistasis and PLINK BOOST identified SNPs within the DRD2 and DRD4 genes, consistent with previously reported genetic associations. Given the variability in tool performance across interaction types, no single method provides optimal detection across all scenarios. Leveraging multiple detection algorithms may therefore yield more comprehensive insights into epistatic effects in quantitative trait analyses. AVAILABILITY AND IMPLEMENTATION: All relevant code and simulated datasets can be found at github.com/staslist/Epistasis_Review repository.

Indexed as

Computational BiologyEpistasis, GeneticPhenotypeQuantitative Trait LociAlgorithmsHumansModels, GeneticPolymorphism, Single Nucleotide

Identifiers

PMID42241225
PMCPMC13264488

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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.