Megavariate methods capture complex genotype-by-environment interactions

被引:0
|
作者
Xavier, Alencar [1 ,2 ]
Runcie, Daniel [3 ]
Habier, David [1 ]
机构
[1] Corteva Agrisci, Seed Prod Dev, 8305 NW 62nd Ave, Johnston, IA 50131 USA
[2] Purdue Univ, Dept Agron, 915 Mitch Daniels Blvd, W Lafayette, IN 47907 USA
[3] Univ Calif Davis, Dept Plant Sci, One Shield Ave, Davis, CA 95616 USA
关键词
accuracy; genomic prediction; multivariate models; matrix decomposition; MIXED-MODEL; VARIANCE-COMPONENTS; MAXIMUM-LIKELIHOOD; PREDICTION; ALGORITHMS; PLANT; INFORMATION; STRATEGIES;
D O I
10.1093/genetics/iyae179
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genomic prediction models that capture genotype-by-environment (GxE) interaction are useful for predicting site-specific performance by leveraging information among related individuals and correlated environments, but implementing such models is computationally challenging. This study describes the algorithm of these scalable approaches, including 2 models with latent representations of GxE interactions, namely MegaLMM and MegaSEM, and an efficient multivariate mixed-model solver, namely Pseudo-expectation Gauss- Seidel (PEGS), fitting different covariance structures [unstructured, extended factor analytic (XFA), Heteroskedastic compound symmetry (HCS)]. Accuracy and runtime are benchmarked on simulated scenarios with varying numbers of genotypes and environments. MegaLMM and PEGS-based XFA and HCS models provided the highest accuracy under sparse testing with 100 testing environments. PEGS-based unstructured model was orders of magnitude fasterthan restricted maximum likelihood (REML) based multivariate genomic best linear unbiased predictions (GBLUP) while providing the same accuracy. MegaSEM provided the lowest runtime, fitting a model with 200 traits and 20,000 individuals in similar to 5 min, and a model with 2,000 traits and 2,000 individuals in less than 3 min. With the genomes-to-fields data, the most accurate predictions were attained with the univariate model fitted across environments and by averaging environment-level genomic estimated breeding values (GEBVs) from models with HCS and XFA covariance structures.
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页数:12
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