ArticleBioinformatics (Oxford, England)2021
A Bayesian linear mixed model for prediction of complex traits.
Article in Bioinformatics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 7 citations in OpenAlex.
- Comparative analysis of four sequencing platforms for methylation sequencing.BMC research notes · 2026Article
- Bayesian variable selection for genome-wide association study of grain traits in rice.PloS one · 2026Article
- Bayesian linear mixed model with multiple random effects for prediction analysis on high-dimensional multi-omics data.Bioinformatics (Oxford, England) · 2023Article
- Bayesian linear mixed model with multiple random effects for family-based genetic studies.Frontiers in genetics · 2023Article
- Explainable deep transfer learning model for disease risk prediction using high-dimensional genomic data.PLoS computational biology · 2022Article
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
motivationAccurate disease risk prediction is essential for precision medicine. Existing models either assume that diseases are caused by groups of predictors with small-to-moderate effects or a few isolated predictors with large effects. Their performance can be sensitive to the underlying disease mechanisms, which are usually unknown in advance.
resultsWe developed a Bayesian linear mixed model (BLMM), where genetic effects were modelled using a hybrid of the sparsity regression and linear mixed model with multiple random effects. The parameters in BLMM were inferred through a computationally efficient variational Bayes algorithm. The proposed method can resemble the shape of the true effect size distributions, captures the predictive effects from both common and rare variants, and is robust against various disease models. Through extensive simulations and the application to a whole-genome sequencing dataset obtained from the Alzheimer's Disease Neuroimaging Initiatives, we have demonstrated that BLMM has better prediction performance than existing methods and can detect variables and/or genetic regions that are predictive. AVAILABILITYAND IMPLEMENTATION: The R-package is available at https://github.com/yhai943/BLMM. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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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.