AI Article Synopsis

  • A simulation study compared Bayesian estimation via Gibbs sampling and empirical BLUP (EBLUP) for analyzing fixed effects and breeding values in animal populations.
  • The study considered various scenarios, including different simulation models, selection schemes, heritability levels, and amounts of missing pedigree information.
  • Results showed that both methods produced similar correlations and patterns of bias and mean square error, with increased estimation error observed as generations progressed or with the presence of missing pedigree data.

Article Abstract

Bayesian (via Gibbs sampling) and empirical BLUP (EBLUP) estimation of fixed effects and breeding values were compared by simulation. Combinations of two simulation models (with or without effect of contemporary group (CG)), three selection schemes (random, phenotypic and BLUP selection), two levels of heritability (0.20 and 0.50) and two levels of pedigree information (0% and 15% randomly missing) were considered. Populations consisted of 450 animals spread over six discrete generations. An infinitesimal additive genetic animal model was assumed while simulating data. EBLUP and Bayesian estimates of CG effects and breeding values were, in all situations, essentially the same with respect to Spearman's rank correlation between true and estimated values. Bias and mean square error (MSE) of EBLUP and Bayesian estimates of CG effects and breeding values showed the same pattern over the range of simulated scenarios. Methods were not biased by phenotypic and BLUP selection when pedigree information was complete, albeit MSE of estimated breeding values increased for situations where CG effects were present. Estimation of breeding values by Bayesian and EBLUP was similarly affected by joint effect of phenotypic or BLUP selection and randomly missing pedigree information. For both methods, bias and MSE of estimated breeding values and CG effects substantially increased across generations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2705422PMC
http://dx.doi.org/10.1186/1297-9686-34-1-41DOI Listing

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