Abstract

BackgroundPedigree-based management of genetic diversity in populations, e.g., using optimal contributions, involves computation of the {mathbf{Ax}} type yielding elements (relationships) or functions (usually averages) of relationship matrices. For pedigree-based relationships {mathbf{A}}, a very efficient method exists. When all the individuals of interest are genotyped, genomic management can be addressed using the genomic relationship matrix {mathbf{G}}; however, to date, the computational problem of efficiently computing {mathbf{Gx}} has not been well studied. When some individuals of interest are not genotyped, genomic management should consider the relationship matrix {mathbf{H}} that combines genotyped and ungenotyped individuals; however, direct computation of {mathbf{Hx}} is computationally very demanding, because construction of a possibly huge matrix is required. Our work presents efficient ways of computing {mathbf{Gx}} and {mathbf{Hx}}, with applications on real data from dairy sheep and dairy goat breeding schemes.ResultsFor genomic relationships, an efficient indirect computation with quadratic instead of cubic cost is {mathbf{x}} = {mathbf{Z}}left( {{mathbf{Z^{prime}x}}} right)/k, where Z is a matrix relating animals to genotypes. For the relationship matrix {mathbf{H}}, we propose an indirect method based on the difference between vectors {mathbf{Hx}} - {mathbf{Ax}}, which involves computation of {mathbf{Ax}} and of products such as {mathbf{Gw}} and {mathbf{A}}_{22}^{ - 1} {mathbf{w}}, where {mathbf{w}} is a working vector derived from {mathbf{x}}. The latter computation is the most demanding but can be done using sparse Cholesky decompositions of matrix {mathbf{A}}^{ - 1}, which allows handling very large genomic and pedigree data files. Studies based on simulations reported in the literature show that the trends of average relationships in {mathbf{H}} and {mathbf{A}} differ as genomic selection proceeds. When selection is based on genomic relationships but management is based on pedigree data, the true genetic diversity is overestimated. However, our tests on real data from sheep and goat obtained before genomic selection started do not show this.ConclusionsWe present efficient methods to compute elements and statistics of the genomic relationships {mathbf{G}} and of matrix {mathbf{H}} that combines ungenotyped and genotyped individuals. These methods should be useful to monitor and handle genomic diversity.

Highlights

  • Pedigree-based management of genetic diversity in populations, e.g., using optimal contributions, involves computation of the Ax type yielding elements or functions of relationship matrices

  • Genomic evaluation considers several tens of thousands of single nucleotide polymorphisms (SNPs) that are distributed across the whole genome, and in the most frequent implementation (genomic best linear unbiased prediction (GBLUP), or single-step GBLUP) it uses a so-called genomic relationship matrix

  • Note that optimal contribution decisions are invariant to the choice of the reference allele or to different estimates of base allelic frequencies used in Z and k, because changing assumed allele frequencies only scale and sum constants to Gx but the optimum is the same

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Summary

Introduction

Pedigree-based management of genetic diversity in populations, e.g., using optimal contributions, involves computation of the Ax type yielding elements (relationships) or functions (usually averages) of relationship matrices. For pedigree-based relationships A, a very efficient method exists. Genomic evaluation considers several tens of thousands of single nucleotide polymorphisms (SNPs) that are distributed across the whole genome, and in the most frequent implementation (genomic best linear unbiased prediction (GBLUP), or single-step GBLUP) it uses a so-called genomic relationship matrix. Following this approach, the accuracy in the evaluation of breeding values is improved compared to that of pedigree-based evaluation by exploiting existing linkage disequilibrium with neighboring quantitative trait loci (QTL) [6]. Genomic selection affects gene transmission, directly for SNPs and indirectly for QTL

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