Abstract

BackgroundMore accurate genomic predictions are expected when the effects of QTL (quantitative trait loci) are predicted from markers in close physical proximity to the QTL. The objective of this study was to quantify to what extent whole-genome methods using 50 K or imputed 770 K SNPs (single nucleotide polymorphisms) could predict single or multiple QTL genotypes based on SNPs in close proximity to those QTL.MethodsPhenotypes with a heritability of 1 were simulated for 2677 Hereford animals genotyped with the BovineSNP50 BeadChip. Genotypes for the high-density 770 K SNP panel were imputed using Beagle software. Various Bayesian regression methods were used to predict single QTL or a trait influenced by 42 such QTL. We quantified to what extent these predictions were based on SNPs in close proximity to the QTL by comparing whole-genome predictions to local predictions based on estimates of the effects of variable numbers of SNPs i.e. ±1, ±2, ±5, ±10, ±50 or ±100 that flanked the QTL.ResultsPrediction accuracies based on local SNPs using whole-genome training for single QTL with the 50 K SNP panel and BayesC0 ranged from 0.49 (±1 SNP) to 0.75 (±100 SNPs). The minimum number of local SNPs for an accurate prediction is ±10 SNPs. Prediction accuracies that were based on local SNPs only were higher than those based on whole-genome SNPs for both 50 K and 770 K SNP panels. For the 770 K SNP panel, prediction accuracies were higher than 0.70 and varied little i.e. between 0.73 (±1 SNP) and 0.77 (±5 SNPs). For the summed 42 QTL, prediction accuracies were generally higher than for single QTL regardless of the number of local SNPs. For QTL with low minor allele frequency (MAF) compared to QTL with high MAF, prediction accuracies increased as the number of SNPs around the QTL increased.ConclusionsThese results suggest that with both 50 K and imputed 770 K SNP genotypes the level of linkage disequilibrium is sufficient to predict single and multiple QTL. However, prediction accuracies are eroded through spuriously estimated effects of SNPs that are distant from the QTL. Prediction accuracies were higher with the 770 K than with the 50 K SNP panel.

Highlights

  • More accurate genomic predictions are expected when the effects of quantitative trait loci (QTL) are predicted from markers in close physical proximity to the QTL

  • Phenotypes used to simulate a single QTL represented the vector of single nucleotide polymorphism (SNP) genotypes at the locus chosen to represent the QTL since multiplying by a simulated QTL effect would scale the vector by a constant

  • Our results suggest that for a dataset with less than 3000 animals, the linkage disequilibrium (LD) of the 50 K SNP panel is sufficient to predict single or multiple QTL

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Summary

Introduction

More accurate genomic predictions are expected when the effects of QTL (quantitative trait loci) are predicted from markers in close physical proximity to the QTL. The objective of this study was to quantify to what extent whole-genome methods using 50 K or imputed 770 K SNPs (single nucleotide polymorphisms) could predict single or multiple QTL genotypes based on SNPs in close proximity to those QTL. The availability of high-density single nucleotide polymorphism (SNP) genotypes across the whole genome has enabled more accurate prediction of breeding values than conventional pedigree-based methods, as well as the mapping of QTL across the genome [4]. Using high-density SNP maps increases the probability of co-segregation between SNPs and quantitative trait nucleotides (QTN) [6]. Since both genomic predictions and genome-wide association studies exploit linkage disequilibrium (LD) between anonymous SNPs and QTN, increasing the density of SNP maps is likely to refine the findings from genome-wide population analyses [7,8,9,10,11]

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