Use este identificador para citar ou linkar para este item: https://locus.ufv.br//handle/123456789/12766
Tipo: Artigo
Título: Genomic prediction for additive and dominance effects of censored traits in pigs
Autor(es): Santos, V.S.
Martins Filho, S.
Resende, M.D.V.
Azevedo, C.F.
Lopes, P.S.
Guimarães, S.E.F.
Silva, F.F.
Abstract: Age at the time of slaughter is a commonly used trait in animal breeding programs. Since studying this trait involves incomplete observations (censoring), analysis can be performed using survival models or modified linear models, for example, by sampling censored data from truncated normal distributions. For genomic selection, the greatest genetic gains can be achieved by including non-additive genetic effects like dominance. Thus, censored traits with effects on both survival models have not yet been studied under a genomic selection approach. We aimed to predict genomic values using the Cox model with dominance effects and compare these results with the linear model with and without censoring. Linear models were fitted via the maximum likelihood method. For censored data, sampling through the truncated normal distribution was used, and the model was called the truncated normal linear via Gibbs sampling (TNL). We used an F2 pig population; the response variable was time (days) from birth to slaughter. Data were previously adjusted for fixed effects of sex and contemporary group. The model predictive ability was calculated based on correlation of predicted genomic values with adjusted phenotypic values. The results showed that both with and without censoring, there was high agreement between Cox and linear models in selection of individuals and markers. Despite including the dominance effect, there was no increase in predictive ability. This study showed, for the first time, the possibility of performing genomic prediction of traits with censored records while using the Cox survival model with additive and dominance effects.
Palavras-chave: GBLUP
Censored data
Mixed model
Survival models
Editor: Genetics and Molecular Research
Tipo de Acesso: Open Access
URI: http://dx.doi.org/10.4238/gmr15048764
http://www.locus.ufv.br/handle/123456789/12766
Data do documento: 17-Out-2016
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