Near-infrared reflectance spectroscopy phenomic prediction can perform similarly to genomic prediction of maize agronomic traits across environments.

Abstract

For nearly two decades, genomic prediction and selection have supported efforts to increase genetic gains in plant and animal improvement programs. However, novel phenomic strategies for predicting complex traits in maize have recently proven beneficial when integrated into across-environment sparse genomic prediction models. One phenomic data modality is whole grain near-infrared spectroscopy (NIRS), which records reflectance values of biological samples (e.g., maize kernels) based on chemical composition. Predictions of hybrid maize grain yield (GY) and 500-kernel weight (KW) across 2 years (2011-2012) and two management conditions (water-stressed and well-watered) were conducted using combinations of reflectance data obtained from high-throughput, F 2 whole-kernel scans and genomic data obtained from genotyping-by-sequencing within four different cross-validation (CV) schemes (CV2, CV1, CV0, and CV00). When predicting the performance of untested genotypes in characterized (CV1) environments, genomic data were better than phenomic data for GY (0.689 ± 0.024-genomic vs. 0.612 ± 0.045-phenomic), but phenomic data were better than genomic data for KW (0.535 ± 0.034-genomic vs. 0.617 ± 0.145-phenomic). Multi-kernel models (combinations of phenomic and genomic relationship matrices) did not surpass single-kernel models for GY prediction in CV1 or CV00 (prediction of untested genotypes in uncharacterized environments); however, these models did outperform the single-kernel models for prediction of KW in these same CVs. Lasso regression applied to the NIRS data set selected a subset of 216 NIRS bands that achieved comparable prediction abilities to the full phenomic data set of 3112 bands predicting GY and KW under CV1 and CV00.

Plant phenotyping relevance

トウモロコシ粒の高スループットNIRS測定と回帰モデルを用いて収量・千粒重を予測し、ゲノム予測との比較検証を行っており、表現型取得・推定法が研究の中心である。

Code and data availability

The paper's data availability statement points to a public GitHub repository containing the annotated R analysis code and all files needed to reproduce the NIRS phenomic and genomic prediction results. The NIRS/phenotype data themselves are from prior works (Lane et al. 2020, Farfan et al. 2015) and no separate public,