| Title: | Efficient penalized generalized linear mixed models for variable selection and genetic risk prediction in high-dimensional data |
| Journal: | Bioinformatics |
| Published: | 27 Jan 2023 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/36708013/ |
| DOI: | https://doi.org/10.1093/bioinformatics/btad063 |
| URL: | https://academic.oup.com/bioinformatics/article-pdf/39/2/btad063/49124083/btad063.pdf |
| Citations: | 5 (5 in last 2 years) as of 8 Aug 2024 |
Publication 7972
WARNING: the interactive features of this website use CSS3, which your browser does not support. To use the full features of this website, please update your browser.
Abstract
MOTIVATION: Sparse 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).</p>
RESULTS: We 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.</p>
AVAILABILITY AND IMPLEMENTATION: Our Julia package PenalizedGLMM.jl is publicly available on github: https://github.com/julstpierre/PenalizedGLMM.</p>
SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.</p>
3 Authors
- Julien St-Pierre
- Karim Oualkacha
- Sahir Rai Bhatnagar
1 Application
| Application ID | Title |
|---|---|
| 20802 | A replication study of pain interactions with comorbidities |
Enabling scientific discoveries that improve human health