Abstract

Official multibreed genomic evaluations for dairy cattle in the United States are based on multibreed BLUP evaluation followed by single-breed estimation of SNP effects. Single-step genomic BLUP (ssGBLUP) allows the straight computation of genomic (G)EBV in a multibreed context. This work aimed to develop ssGBLUP multibreed genomic predictions for US dairy cattle using the algorithm for proven and young (APY) to compute the inverse of the genomic relationship matrix. Only purebred Ayrshire (AY), Brown Swiss (BS), Guernsey (GU), Holstein (HO), and Jersey (JE) animals were considered. A 3-trait model with milk (MY), fat (FY), and protein (PY) yields was applied using about 45 million phenotypes recorded from January 2000 to June 2020. The whole data set included about 29.5 million animals, of which almost 4 million were genotyped. All the effects in the model were breed specific, and breed was also considered as fixed unknown parent groups. Evaluations were done for (1) each single breed separately (single); (2) HO and JE together (HO_JE); (3) AY, BS, and GU together (AY_BS_GU); (4) all the 5 breeds together (5_BREEDS). Initially, 15k core animals were used in APY for AY_BS_GU and 5_BREEDS, but larger core sets with more animals from the least represented breeds were also tested. The HO_JE evaluation had a fixed set of 30k core animals, with an equal representation of the 2 breeds, whereas HO and JE single-breed analysis involved 15k core animals. Validation for cows was based on correlations between adjusted phenotypes and (G)EBV, whereas for bulls on the regression of daughter yield deviations on (G)EBV. Because breed was correctly considered in the model, BLUP results for single and multibreed analyses were the same. Under ssGBLUP, predictability and reliability for AY, BS, and GU were on average 7% and 2% lower in 5_BREEDS compared with single-breed evaluations, respectively. However, validation parameters for these 3 breeds became better than in the single-breed evaluations when 45k animals were included in the core set for 5_BREEDS. Evaluations for Holsteins were more stable across scenarios because of the greatest number of genotyped animals and amount of data. Combining AY, BS, and GU into one evaluation resulted in predictions similar to the ones from single breed, especially when using about 30k core animals in APY. The results showed that single-step large-scale multibreed evaluations are computationally feasible, but fine tuning is needed to avoid a reduction in reliability when numerically dominant breeds are combined. Having evaluations for AY, BS, and GU separated from HO and JE may reduce inflation of GEBV for the first 3 breeds.

Highlights

  • Official multibreed genomic evaluations for dairy cattle in the United States are based on multibreed BLUP evaluations followed by single-breed estimation of SNP effects

  • Since animals were not connected by the pedigree and the breed was correctly accounted for by the model, BLUP results for single and all multibreed scenarios were the same: correlations between raw EBVs estimated in BLUP single and BLUP multibreed were 1.00 for all breeds and traits

  • Correlations between raw GEBVs estimated in Single-step genomic BLUP (ssGBLUP) single and ssGBLUP 5_BREEDS_45k ranged from 0.95 (MY for AY and Brown Swiss (BS)) to 1

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Summary

Introduction

Official multibreed genomic evaluations for dairy cattle in the United States are based on multibreed BLUP evaluations followed by single-breed estimation of SNP effects. This is the so-called multistep method (VanRaden, 2008; VanRaden et al, 2009), where genomic PTA is obtained as the combination of direct genomic value based on markers and parent average. The effectiveness of genomic evaluations relies on the availability of a large reference population where the marker effects can be estimated (Goddard, 2009). The accuracy of this estimation strongly depends on the size of the reference population. The availability of genotypes drastically increased and the number of animals with genomic information recently hit 5 million only in the United States (https://queries.uscdcb.com/Genotype/counts.html)

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