ArticlePLoS genetics2020
Simultaneous SNP selection and adjustment for population structure in high dimensional prediction models.
Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.
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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.
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Who cites it
7 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Fully exploiting SNP arrays: a systematic review on the tools to extract underlying genomic structure.Briefings in bioinformatics · 2022Pooled it
- plmmr: an R package to fit penalized linear mixed models for genome-wide association data with complex correlation structure.Briefings in bioinformatics · 2026Article
- Hierarchical selection of genetic and gene by environment interaction effects in high-dimensional mixed models.Statistical methods in medical research · 2025Review
- High-dimensional supervised classification in a context of non-independence of observations to identify the determining SNPs in a phenotype.Infectious Disease Modelling · 2023Article
- Efficient penalized generalized linear mixed models for variable selection and genetic risk prediction in high-dimensional data.Bioinformatics (Oxford, England) · 2023Article
- Fast and efficient correction for population stratification in multi-locus genome-wide association studies.Genetica · 2021Article
- Penalized linear mixed models for structured genetic data.Genetic epidemiology · 2021Review
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
Complex traits are known to be influenced by a combination of environmental factors and rare and common genetic variants. However, detection of such multivariate associations can be compromised by low statistical power and confounding by population structure. Linear mixed effects models (LMM) can account for correlations due to relatedness but have not been applicable in high-dimensional (HD) settings where the number of fixed effect predictors greatly exceeds the number of samples. False positives or false negatives can result from two-stage approaches, where the residuals estimated from a null model adjusted for the subjects' relationship structure are subsequently used as the response in a standard penalized regression model. To overcome these challenges, we develop a general penalized LMM with a single random effect called ggmix for simultaneous SNP selection and adjustment for population structure in high dimensional prediction models. We develop a blockwise coordinate descent algorithm with automatic tuning parameter selection which is highly scalable, computationally efficient and has theoretical guarantees of convergence. Through simulations and three real data examples, we show that ggmix leads to more parsimonious models compared to the two-stage approach or principal component adjustment with better prediction accuracy. Our method performs well even in the presence of highly correlated markers, and when the causal SNPs are included in the kinship matrix. ggmix can be used to construct polygenic risk scores and select instrumental variables in Mendelian randomization studies. Our algorithms are available in an R package available on CRAN (https://cran.r-project.org/package=ggmix).
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Registered trials
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.