Abstract

A barrier to the adoption of genomic prediction in small breeding programs is the initial cost of genotyping material. Although decreasing, marker costs are usually higher than field trial costs. In this study we demonstrate the utility of stratifying a narrow‐base biparental oat population genotyped with a modest number of markers to employ genomic prediction at early and later generations. We also show that early generation genotyping data can reduce the number of lines for later phenotyping based on selections of siblings to progress. Using sets of small families selected at an early generation could enable the use of genomic prediction for adaptation to multiple target environments at an early stage in the breeding program. In addition, we demonstrate that mixed marker data can be effectively integrated to combine cheap dominant marker data (including legacy data) with more expensive but higher density codominant marker data in order to make within generation and between lineage predictions based on genotypic information. Taken together, our results indicate that small programs can test and initiate genomic predictions using sets of stratified, narrow‐base populations and incorporating low density legacy genotyping data. This can then be scaled to include higher density markers and a broadened population base.

Highlights

  • The adoption of affordable genetic markers in breeding programs has expanded the use of accelerated, genomic-based breeding approaches from genome-wide information (Lorenzana & Bernardo, 2009; Morrell, Buckler, & Ross-Ibarra, Abbreviations: best linear unbiased prediction (BLUP), Best linear unbiased prediction; CV, Cross-validation; DArT, Diversity Array Technology; differentially penalized regression (DiPR), Differentially penalized ridge regression; GBS, Genotyping-by-sequencing; genomic estimated breeding value (GEBV), Genomic estimated breeding value; GS, Genomic selection; linkage disequilibrium (LD), Linkage disequilibrium; MCCV, Monte Carlo cross-validation; recombinant inbred lines (RILs), Recombinant inbred line; RR-BLUP, Ridge regression-BLUP; SSD, Single-seed descent; single nucleotide polymorphisms (SNPs), single nucleotide polymorphism.2011)

  • Using low-coverage genotypic information in the early generation, we investigate the recovery of missing phenotypes via genomic prediction, which is required for accurate representation of true phenotypic value and variance

  • We demonstrate that it is feasible to use the genotypic information from a full set of biparental lines to make within generation, betweenlineage genomic predictions

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Summary

Introduction

The adoption of affordable genetic markers in breeding programs has expanded the use of accelerated, genomic-based breeding approaches from genome-wide information (Lorenzana & Bernardo, 2009; Morrell, Buckler, & Ross-Ibarra, Abbreviations: BLUP, Best linear unbiased prediction; CV, Cross-validation; DArT, Diversity Array Technology; DiPR, Differentially penalized ridge regression; GBS, Genotyping-by-sequencing; GEBV, Genomic estimated breeding value; GS, Genomic selection; LD, Linkage disequilibrium; MCCV, Monte Carlo cross-validation; RIL, Recombinant inbred line; RR-BLUP, Ridge regression-BLUP; SSD, Single-seed descent; SNP, single nucleotide polymorphism.2011). Ongoing research in crops has progressed beyond improving prediction accuracy and centers on how best to employ GS within breeding programs (Arruda et al, 2015; Bassi, Bentley, Charmet, Ortiz, & Crossa, 2015; Jarquín et al, 2016; Norman, Taylor, Edwards, & Kuchel, 2018; Vivek et al, 2017), the transition to practical implementation in small programs remains a challenge (Voss-Fels, Cooper, & Hayes, 2019). This is predominantly due to the initial expense. In small programs, the gradual generation and use of genotypic data in narrow-based populations can support the longer-term adoption of GS

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