ArticleBioinformatics (Oxford, England)2023
Efficient penalized generalized linear mixed models for variable selection and genetic risk prediction in high-dimensional data.
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 9 papers.
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9 citing papers in PubMed.
- D3MI: an efficient and powerful federated imputation method for bias reduction in the analysis of distributed incomplete data by accounting for within-site correlation and between-site heterogeneity.BMC medical informatics and decision making · 2026Article
- Boolean logic links chromatin accessibility states to gene expression variability across cell types.Nucleic acids research · 2026Article
- plmmr: an R package to fit penalized linear mixed models for genome-wide association data with complex correlation structure.Briefings in bioinformatics · 2026Article
- Longitudinal omics data analysis: approaches and applications.Computational and structural biotechnology journal · 2026Review
- HighDimMixedModels.jl: Robust high-dimensional mixed-effects models across omics data.PLoS computational biology · 2025Article
- Hierarchical selection of genetic and gene by environment interaction effects in high-dimensional mixed models.Statistical methods in medical research · 2025Review
- Review on GPU accelerated methods for genome-wide SNP-SNP interactions.Molecular genetics and genomics : MGG · 2024Review
- Bayesian bi-level variable selection for genome-wide survival study.Genomics & informatics · 2023Article
- Graph Regression Model for Spatial and Temporal Environmental Data-Case of Carbon Dioxide Emissions in the United States.Entropy (Basel, Switzerland) · 2023Article
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3 authors.
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Abstract
motivationSparse regularized regression methods are now widely used in genome-wide association studies (GWAS) to address the multiple testing burden that limits discovery of potentially important predictors. Linear mixed models (LMMs) have become an attractive alternative to principal components (PCs) adjustment to account for population structure and relatedness in high-dimensional penalized models. However, their use in binary trait GWAS rely on the invalid assumption that the residual variance does not depend on the estimated regression coefficients. Moreover, LMMs use a single spectral decomposition of the covariance matrix of the responses, which is no longer possible in generalized linear mixed models (GLMMs).
resultsWe introduce a new method called pglmm, a penalized GLMM that allows to simultaneously select genetic markers and estimate their effects, accounting for between-individual correlations and binary nature of the trait. We develop a computationally efficient algorithm based on penalized quasi-likelihood estimation that allows to scale regularized mixed models on high-dimensional binary trait GWAS. We show through simulations that when the dimensionality of the relatedness matrix is high, penalized LMM and logistic regression with PC adjustment fail to select important predictors, and have inferior prediction accuracy compared to pglmm. Further, we demonstrate through the analysis of two polygenic binary traits in a subset of 6731 related individuals from the UK Biobank data with 320K SNPs that our method can achieve higher predictive performance, while also selecting fewer predictors than a sparse regularized logistic lasso with PC adjustment. AVAILABILITY AND IMPLEMENTATION: Our Julia package PenalizedGLMM.jl is publicly available on github: https://github.com/julstpierre/PenalizedGLMM. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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