| Title: | Stochastic Lanczos estimation of genomic variance components for linear mixed-effects models |
| Journal: | BMC Bioinformatics |
| Published: | 30 Jul 2019 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/31362713/ |
| DOI: | https://doi.org/10.1186/s12859-019-2978-z |
| Citations: | 5 (1 in last 2 years) as of 8 Aug 2024 |
Publication 7510
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Abstract
BackgroundLinear mixed-effects models (LMM) are a leading method in conducting genome-wide association studies (GWAS) but require residual maximum likelihood (REML) estimation of variance components, which is computationally demanding. Previous work has reduced the computational burden of variance component estimation by replacing direct matrix operations with iterative and stochastic methods and by employing loose tolerances to limit the number of iterations in the REML optimization procedure. Here, we introduce two novel algorithms, stochastic Lanczos derivative-free REML (SLDF_REML) and Lanczos first-order Monte Carlo REML (L_FOMC_REML), that exploit problem structure via the principle of Krylov subspace shift-invariance to speed computation beyond existing methods. Both novel algorithms only require a single round of computation involving iterative matrix operations, after which their respective objectives can be repeatedly evaluated using vector operations. Further, in contrast to existing stochastic methods, SLDF_REML can exploit precomputed genomic relatedness matrices (GRMs), when available, to further speed computation.ResultsResults of numerical experiments are congruent with theory and demonstrate that interpreted-language implementations of both algorithms match or exceed existing compiled-language software packages in speed, accuracy, and flexibility.ConclusionsBoth the SLDF_REML and L_FOMC_REML algorithms outperform existing methods for REML estimation of variance components for LMM and are suitable for incorporation into existing GWAS LMM software implementations.2 Authors
- Richard Border
- Stephen Becker
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