Abstract

BackgroundAt the current price, the use of high-density single nucleotide polymorphisms (SNP) genotyping assays in genomic selection of dairy cattle is limited to applications involving elite sires and dams. The objective of this study was to evaluate the use of low-density assays to predict direct genomic value (DGV) on five milk production traits, an overall conformation trait, a survival index, and two profit index traits (APR, ASI).MethodsDense SNP genotypes were available for 42,576 SNP for 2,114 Holstein bulls and 510 cows. A subset of 1,847 bulls born between 1955 and 2004 was used as a training set to fit models with various sets of pre-selected SNP. A group of 297 bulls born between 2001 and 2004 and all cows born between 1992 and 2004 were used to evaluate the accuracy of DGV prediction. Ridge regression (RR) and partial least squares regression (PLSR) were used to derive prediction equations and to rank SNP based on the absolute value of the regression coefficients. Four alternative strategies were applied to select subset of SNP, namely: subsets of the highest ranked SNP for each individual trait, or a single subset of evenly spaced SNP, where SNP were selected based on their rank for ASI, APR or minor allele frequency within intervals of approximately equal length.ResultsRR and PLSR performed very similarly to predict DGV, with PLSR performing better for low-density assays and RR for higher-density SNP sets. When using all SNP, DGV predictions for production traits, which have a higher heritability, were more accurate (0.52-0.64) than for survival (0.19-0.20), which has a low heritability. The gain in accuracy using subsets that included the highest ranked SNP for each trait was marginal (5-6%) over a common set of evenly spaced SNP when at least 3,000 SNP were used. Subsets containing 3,000 SNP provided more than 90% of the accuracy that could be achieved with a high-density assay for cows, and 80% of the high-density assay for young bulls.ConclusionsAccurate genomic evaluation of the broader bull and cow population can be achieved with a single genotyping assays containing ~ 3,000 to 5,000 evenly spaced SNP.

Highlights

  • At the current price, the use of high-density single nucleotide polymorphisms (SNP) genotyping assays in genomic selection of dairy cattle is limited to applications involving elite sires and dams

  • Accuracy of direct genomic value (DGV) prediction from the analysis of all 42,576 SNP ranged from 0.15 to 0.64 for RR and 0.20 to 0.64 for partial least squares regression (PLSR) in the validation set of bulls, and from 0.22 to 0.57 for RR and from 0.21 to 0.54 for PLSR in the validation set of cows (Figure 2)

  • Irrespective of the method of SNP selection, subsets containing 3,000 SNP provided more than 90% of the accuracy that could be achieved with a high-density assay for cows, and 80% for young bulls

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Summary

Introduction

The use of high-density single nucleotide polymorphisms (SNP) genotyping assays in genomic selection of dairy cattle is limited to applications involving elite sires and dams. Significant additional gains in GS schemes could be made if cows to breed sires and cows to breed cows were selected on genomic breeding values [1]. Another benefit of genotyping cows may be lower rates of inbreeding: according to Daetwyler et al [3], the use of GS. High-density SNP genotyping assays are limited to applications involving elite sires and dams. The use of such a low-density array may still be limited if multiple traits require so many SNP that their genotyping cost is similar to the cost of a high-density chip

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