Abstract

An increased availability of genotypes at marker loci has prompted the development of models that include the effect of individual genes. Selection based on these models is known as marker-assisted selection (MAS). MAS is known to be efficient especially for traits that have low heritability and non-additive gene action. BLUP methodology under non-additive gene action is not feasible for large inbred or crossbred pedigrees. It is easy to incorporate non-additive gene action in a finite locus model. Under such a model, the unobservable genotypic values can be predicted using the conditional mean of the genotypic values given the data. To compute this conditional mean, conditional genotype probabilities must be computed. In this study these probabilities were computed using iterative peeling, and three Markov chain Monte Carlo (MCMC) methods – scalar Gibbs, blocking Gibbs, and a sampler that combines the Elston Stewart algorithm with iterative peeling (ESIP). The performance of these four methods was assessed using simulated data. For pedigrees with loops, iterative peeling fails to provide accurate genotype probability estimates for some pedigree members. Also, computing time is exponentially related to the number of loci in the model. For MCMC methods, a linear relationship can be maintained by sampling genotypes one locus at a time. Out of the three MCMC methods considered, ESIP, performed the best while scalar Gibbs performed the worst.

Highlights

  • Marker assisted genetic evaluation (MAGE) is most useful for traits with low heritability [23,27] that exhibit non-additive gene action [6]

  • For the onelocus models considered in our study, Figure 2 indicates that for quantitative traits iterative peeling can yield absolute errors that are larger than 0.1 genetic standard deviations

  • A linear relationship between computing efficiency and the number of loci can be maintained for Markov chain Monte Carlo (MCMC) methods by sampling one locus at a time

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Summary

Introduction

Marker assisted genetic evaluation (MAGE) is most useful for traits with low heritability [23,27] that exhibit non-additive gene action [6]. To overcome the computing problems associated with BLUP under non-additive gene action, it has been proposed to predict the unobservable genotypic values using the conditional mean of the genotypic values given the data, calculated under the assumption of a finite locus model [14,19,28]. The appropriateness of finite locus models for genetic evaluation for quantitative traits is currently under investigation, and preliminary results indicate that models with 2–10 loci yield evaluations that are practically indistinguishable from BLUP evaluations [30,31]

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