Improving Genomic Prediction Using High-Dimensional Secondary Phenotypes

Frontiers in Genetics

Bader Arouisse¹  Fred A. van Eeuwijk¹  Willem Kruijer¹  Tom P. J. M. Theeuwen² 

[1] Biometris, Wageningen University and Research, Wageningen, Netherlands;Laboratory of Genetics, Wageningen University and Research, Wageningen, Netherlands;

关键词: GBLUP;    genomic prediction;    secondary traits;    selection indices;    penalized regression;    random forest;   

DOI  :  10.3389/fgene.2021.667358

来源: DOAJ

【 摘 要 】

In the past decades, genomic prediction has had a large impact on plant breeding. Given the current advances of high-throughput phenotyping and sequencing technologies, it is increasingly common to observe a large number of traits, in addition to the target trait of interest. This raises the important question whether these additional or “secondary” traits can be used to improve genomic prediction for the target trait. With only a small number of secondary traits, this is known to be the case, given sufficiently high heritabilities and genetic correlations. Here we focus on the more challenging situation with a large number of secondary traits, which is increasingly common since the arrival of high-throughput phenotyping. In this case, secondary traits are usually incorporated through additional relatedness matrices. This approach is however infeasible when secondary traits are not measured on the test set, and cannot distinguish between genetic and non-genetic correlations. An alternative direction is to extend the classical selection indices using penalized regression. So far, penalized selection indices have not been applied in a genomic prediction setting, and require plot-level data in order to reliably estimate genetic correlations. Here we aim to overcome these limitations, using two novel approaches. Our first approach relies on a dimension reduction of the secondary traits, using either penalized regression or random forests (LS-BLUP/RF-BLUP). We then compute the bivariate GBLUP with the dimension reduction as secondary trait. For simulated data (with available plot-level data), we also use bivariate GBLUP with the penalized selection index as secondary trait (SI-BLUP). In our second approach (GM-BLUP), we follow existing multi-kernel methods but replace secondary traits by their genomic predictions, with the advantage that genomic prediction is also possible when secondary traits are only measured on the training set. For most of our simulated data, SI-BLUP was most accurate, often closely followed by RF-BLUP or LS-BLUP. In real datasets, involving metabolites in Arabidopsis and transcriptomics in maize, no method could substantially improve over univariate prediction when secondary traits were only available on the training set. LS-BLUP and RF-BLUP were most accurate when secondary traits were available also for the test set.

【 授权许可】

Unknown