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Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments
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Abstract
We compared the predictive ability of various prediction models for a maize dataset derived from 910 doubled haploid lines from European landraces (Kemater Landmais Gelb and Petkuser Ferdinand Rot), which were tested in six locations in Germany and Spain. The compared models were Genomic Best Linear Unbiased Prediction (GBLUP) as an additive model, Epistatic Random Regression BLUP (ERRBLUP) accounting for all pairwise SNP interactions, and selective Epistatic Random Regression BLUP (sERRBLUP) accounting for a selected subset of pairwise SNP interactions. These models have been compared in both univariate and bivariate statistical settings within and across environments. Our results indicate that modeling all pairwise SNP interactions into the univariate/bivariate model (ERRBLUP) is not superior in predictive ability to the respective additive model (GBLUP). However, incorporating only a selected subset of interactions with the highest effect variances in univariate/bivariate sERRBLUP can increase predictive ability significantly compared to the univariate/bivariate GBLUP. Overall, bivariate models consistently outperform univariate models in predictive ability. Over all studied traits, locations, and landraces, the increase in prediction accuracy from univariate GBLUP to univariate sERRBLUP ranged from 5.9 to 112.4 percent, with an average increase of 47 percent. For bivariate models, the change ranged from −0.3 to +27.9 percent comparing the bivariate sERRBLUP to the bivariate GBLUP. The average increase across traits and locations was 11 percent. This considerable increase in predictive ability achieved by sERRBLUP may be of interest for “sparse testing” approaches in which only a subset of the lines/hybrids of interest is observed at each location.
Key Message
The prediction accuracy of genomic prediction of phenotypes can be increased by only including top ranked pairwise SNP interactions into the prediction models.
Title: Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments
Description:
Abstract
We compared the predictive ability of various prediction models for a maize dataset derived from 910 doubled haploid lines from European landraces (Kemater Landmais Gelb and Petkuser Ferdinand Rot), which were tested in six locations in Germany and Spain.
The compared models were Genomic Best Linear Unbiased Prediction (GBLUP) as an additive model, Epistatic Random Regression BLUP (ERRBLUP) accounting for all pairwise SNP interactions, and selective Epistatic Random Regression BLUP (sERRBLUP) accounting for a selected subset of pairwise SNP interactions.
These models have been compared in both univariate and bivariate statistical settings within and across environments.
Our results indicate that modeling all pairwise SNP interactions into the univariate/bivariate model (ERRBLUP) is not superior in predictive ability to the respective additive model (GBLUP).
However, incorporating only a selected subset of interactions with the highest effect variances in univariate/bivariate sERRBLUP can increase predictive ability significantly compared to the univariate/bivariate GBLUP.
Overall, bivariate models consistently outperform univariate models in predictive ability.
Over all studied traits, locations, and landraces, the increase in prediction accuracy from univariate GBLUP to univariate sERRBLUP ranged from 5.
9 to 112.
4 percent, with an average increase of 47 percent.
For bivariate models, the change ranged from −0.
3 to +27.
9 percent comparing the bivariate sERRBLUP to the bivariate GBLUP.
The average increase across traits and locations was 11 percent.
This considerable increase in predictive ability achieved by sERRBLUP may be of interest for “sparse testing” approaches in which only a subset of the lines/hybrids of interest is observed at each location.
Key Message
The prediction accuracy of genomic prediction of phenotypes can be increased by only including top ranked pairwise SNP interactions into the prediction models.
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