Abstract

ABSTRACTWe combined linkage (LA) and linkage disequilibrium (LDA) analyses (emerging the term ‘LALDA’) for genomic selection (GS) purposes. The models were fitted to a simulated dataset and to a real data of feed conversion ratio in pigs. Firstly, the significant QTLs (quantitative trait locus) were identified through LA-based mixed models considering the QTL-genotypes as random effects by means of genotypic identity by descent matrix. This matrix was calculated at the positions of significant QTLs (based on LA) allowing to include the QTL-genotype effects additionally to SNP (single nucleotide polymorphism) markers (based on LDA) and additive polygenic effects in several GS models (Bayesian Ridge Regression – BRR; Bayes A – BA; Bayes B – BB; Bayes C – BC and Bayesian LASSO – BL). These models combing all mentioned effects were denominated LALDA. Goodness-of-fit and predictive ability analyses were performed to evaluate the efficiency of these models. For the real data, although slightly, the superiority of the LALDA models was verified in comparison to traditional LDA models for GS. For the simulated dataset, the models presented similar results. For both LDA and LALDA frameworks, BA showed the best fitting through Deviance Information Criterion and higher predictive ability in the simulated and real datasets.

Highlights

  • Linkage disequilibrium analysis (LDA) is the basic concept behind genomic selection (GS), since the associations between markers and QTLs is an attribute of the population as a whole

  • We aimed to propose and test a new class of Bayesian LALDA models for genomic selection implemented through free software (QXPAK e R)

  • As the QTLs are assumed as specific SNPs, these markers were excluded from the LDA component of the LALDA model, being considered only in the linkage analysis (LA) component

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Summary

Introduction

Linkage disequilibrium analysis (LDA) is the basic concept behind genomic selection (GS), since the associations between markers and QTLs (quantitative trait locus) is an attribute of the population as a whole. For this reason, it is expected that these associations be shared by all individuals of the population and be preserved for several generations. Wientjes et al (2013) reported that prediction accuracy in GS depends on linkage disequilibrium from recent familiar structures, signalling for the contribution of LA for GS. According to Bercovici et al (2010), these regions are better candidates for detection of causal mutations affecting the phenotypes, and can be exploited under a genome-enabled prediction viewpoint

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