Literature DB >> 18272854

Estimation of accuracy and bias in genetic evaluations with genetic groups using sampling.

J M Hickey1, M G Keane, D A Kenny, A R Cromie, H A Mulder, R F Veerkamp.   

Abstract

Accuracy and bias of EBV are important measures of the quality of genetic evaluations. A sampling method that accounts for the uncertainty in the estimation of genetic group effects was used to calculate accuracy and bias of estimated effects. The method works by repeatedly simulating phenotypes for multiple traits for a defined data and pedigree structure. These simulated values are analyzed using BLUP with genetic groups in the relationship matrix. Accuracies and biases are then calculated as correlations among and differences between true and estimated values across all replicates, respectively. The method was applied to the Irish beef production data set for 15 traits and with 15 genetic groups to account for differences in breed means. Accuracy and bias of estimated genetic group effects, estimated comparisons between genetic group effects, EBV within genetic group, and EBV across genetic group were calculated. Small biases were detected for most estimated genetic group effects and most estimated comparisons between genetic group effects. Most of these were not important relative to the phenotypic SD of the traits involved. For example, a bias of 0.78% of the phenotypic SD was detected for carcass conformation in Aberdeen Angus. However, one trait, calf quality, which had few performance records in the data set, displayed larger bias, ranging from -10.31 to 5.85% of the phenotypic SD across the different estimated genetic group effects. Large differences were observed in the accuracies of genetic group effects, ranging from 0.02 for feed intake in Holstein, which had no data recorded, to >0.97 for carcass conformation, a trait with large amounts of data recorded in the different genetic groups. Large differences were also observed in the accuracies of the comparisons among genetic group effects. The accuracies of the EBV within genetic group and EBV across genetic group were sometimes different; for example, carcass conformation in Belgian Blue had an average accuracy within genetic group of 0.69 compared with an average accuracy across genetic group of 0.89. This suggests that the accuracy of genetic groups should be taken into account when publishing EBV across genetic groups.

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Year:  2008        PMID: 18272854     DOI: 10.2527/jas.2007-0653

Source DB:  PubMed          Journal:  J Anim Sci        ISSN: 0021-8812            Impact factor:   3.159


  2 in total

1.  Arsenic trioxide inhibits EBV reactivation and promotes cell death in EBV-positive lymphoma cells.

Authors:  Qinyan Yin; Mark Sides; Christopher H Parsons; Erik K Flemington; Joseph A Lasky
Journal:  Virol J       Date:  2017-06-21       Impact factor: 4.099

2.  Estimation of prediction error variances via Monte Carlo sampling methods using different formulations of the prediction error variance.

Authors:  John M Hickey; Roel F Veerkamp; Mario P L Calus; Han A Mulder; Robin Thompson
Journal:  Genet Sel Evol       Date:  2009-02-09       Impact factor: 4.297

  2 in total

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