Evidence map›Paper›PMID 36708013›Full record

ArticleBioinformatics (Oxford, England)2023

Efficient penalized generalized linear mixed models for variable selection and genetic risk prediction in high-dimensional data.

Julien St-Pierre, Karim Oualkacha, Sahir Rai Bhatnagar

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
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  4. Longitudinal omics data analysis: approaches and applications.Computational and structural biotechnology journal · 2026
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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.

Julien St-PierreDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, QC H3A 1G1, Canada.ORCID 0000-0001-9627-576X
Karim OualkachaDépartement de Mathématiques, Université du Québec à Montréal, Montréal, QC H2X 3Y7, Canada.ORCID 0000-0002-9911-079X
Sahir Rai BhatnagarDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, QC H3A 1G1, Canada.ORCID 0000-0001-8956-2509

Funding

Fonds de recherche Québec-Santé 267074Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Natural Sciences and Engineering Research Council of Canada RGPIN-2019-06727
6 · The paper itself

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.

Indexed as

AlgorithmsGenome-Wide Association StudyHumansLinear ModelsModels, GeneticPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID36708013
PMCPMC9907224

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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.