Genomic selection for slaughter age in pigs using the Cox frailty model.
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
Texto Completo: | http://dx.doi.org/10.4238/2015.October.19.5 http://www.alice.cnptia.embrapa.br/alice/handle/doc/1030248 |
Resumo: | The aim of this study was to compare genomic selection methodologies using a linear mixed model and the Cox survival model. We used data from an F2 population of pigs, in which the response variable was the time in days from birth to the culling of the animal and the covariates were 238 markers [237 single nucleotide polymorphism (SNP) plus the halothane gene]. The data were corrected for fixed effects, and the accuracy of the method was determined based on the correlation of the ranks of predicted genomic breeding values (GBVs) in both models with the corrected phenotypic values. The analysis was repeated with a subset of SNP markers with largest absolute effects. The results were in agreement with the GBV prediction and the estimation of marker effects for both models for uncensored data and for normality. However, when considering censored data, the Cox model with a normal random effect (S1) was more appropriate. Since there was no agreement between the linear mixed model and the imputed data (L2) for the prediction of genomic values and the estimation of marker effects, the model S1 was considered superior as it took into account the latent variable and the censored data. Marker selection increased correlations between the ranks of predicted GBVs by the linear and Cox frailty models and the corrected phenotypic values, and 120 markers were required to increase the predictive ability for the characteristic analyzed. |
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Genomic selection for slaughter age in pigs using the Cox frailty model.Dado censuradoModelo mixtoCensured dataMixed modelPolimorfismopolymorphismThe aim of this study was to compare genomic selection methodologies using a linear mixed model and the Cox survival model. We used data from an F2 population of pigs, in which the response variable was the time in days from birth to the culling of the animal and the covariates were 238 markers [237 single nucleotide polymorphism (SNP) plus the halothane gene]. The data were corrected for fixed effects, and the accuracy of the method was determined based on the correlation of the ranks of predicted genomic breeding values (GBVs) in both models with the corrected phenotypic values. The analysis was repeated with a subset of SNP markers with largest absolute effects. The results were in agreement with the GBV prediction and the estimation of marker effects for both models for uncensored data and for normality. However, when considering censored data, the Cox model with a normal random effect (S1) was more appropriate. Since there was no agreement between the linear mixed model and the imputed data (L2) for the prediction of genomic values and the estimation of marker effects, the model S1 was considered superior as it took into account the latent variable and the censored data. Marker selection increased correlations between the ranks of predicted GBVs by the linear and Cox frailty models and the corrected phenotypic values, and 120 markers were required to increase the predictive ability for the characteristic analyzed.V. S. SANTOS, Universidade Federal de Viçosa; S. MARTINS FILHO, Universidade Federal de Viçosa; MARCOS DEON VILELA DE RESENDE, CNPF; C. F. AZEVEDO, Universidade Federal de Viçosa; P. S. LOPES, Universidade Federal de Viçosa; S. E. F. GUIMARAES, Universidade Federal de Viçosa; L. S. GLORIA, Universidade Federal de Viçosa; F. F. SILVA, Universidade Federal de Viçosa.SANTOS, V. S.MARTINS FILHO, S.RESENDE, M. D. V. deAZEVEDO, C. F.LOPES, P. S.GUIMARAES, S. E. F.GLORIA, L. S.SILVA, F. F.2018-01-03T23:17:47Z2018-01-03T23:17:47Z2015-12-0220152018-01-03T23:17:47Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleGenetics and Molecular Research, Ribeirão Preto, v. 14, n. 4, p. 12616-12627, 2015.http://dx.doi.org/10.4238/2015.October.19.5http://www.alice.cnptia.embrapa.br/alice/handle/doc/1030248enginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2018-01-03T23:17:54Zoai:www.alice.cnptia.embrapa.br:doc/1030248Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542018-01-03T23:17:54falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542018-01-03T23:17:54Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false |
dc.title.none.fl_str_mv |
Genomic selection for slaughter age in pigs using the Cox frailty model. |
title |
Genomic selection for slaughter age in pigs using the Cox frailty model. |
spellingShingle |
Genomic selection for slaughter age in pigs using the Cox frailty model. SANTOS, V. S. Dado censurado Modelo mixto Censured data Mixed model Polimorfismo polymorphism |
title_short |
Genomic selection for slaughter age in pigs using the Cox frailty model. |
title_full |
Genomic selection for slaughter age in pigs using the Cox frailty model. |
title_fullStr |
Genomic selection for slaughter age in pigs using the Cox frailty model. |
title_full_unstemmed |
Genomic selection for slaughter age in pigs using the Cox frailty model. |
title_sort |
Genomic selection for slaughter age in pigs using the Cox frailty model. |
author |
SANTOS, V. S. |
author_facet |
SANTOS, V. S. MARTINS FILHO, S. RESENDE, M. D. V. de AZEVEDO, C. F. LOPES, P. S. GUIMARAES, S. E. F. GLORIA, L. S. SILVA, F. F. |
author_role |
author |
author2 |
MARTINS FILHO, S. RESENDE, M. D. V. de AZEVEDO, C. F. LOPES, P. S. GUIMARAES, S. E. F. GLORIA, L. S. SILVA, F. F. |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
V. S. SANTOS, Universidade Federal de Viçosa; S. MARTINS FILHO, Universidade Federal de Viçosa; MARCOS DEON VILELA DE RESENDE, CNPF; C. F. AZEVEDO, Universidade Federal de Viçosa; P. S. LOPES, Universidade Federal de Viçosa; S. E. F. GUIMARAES, Universidade Federal de Viçosa; L. S. GLORIA, Universidade Federal de Viçosa; F. F. SILVA, Universidade Federal de Viçosa. |
dc.contributor.author.fl_str_mv |
SANTOS, V. S. MARTINS FILHO, S. RESENDE, M. D. V. de AZEVEDO, C. F. LOPES, P. S. GUIMARAES, S. E. F. GLORIA, L. S. SILVA, F. F. |
dc.subject.por.fl_str_mv |
Dado censurado Modelo mixto Censured data Mixed model Polimorfismo polymorphism |
topic |
Dado censurado Modelo mixto Censured data Mixed model Polimorfismo polymorphism |
description |
The aim of this study was to compare genomic selection methodologies using a linear mixed model and the Cox survival model. We used data from an F2 population of pigs, in which the response variable was the time in days from birth to the culling of the animal and the covariates were 238 markers [237 single nucleotide polymorphism (SNP) plus the halothane gene]. The data were corrected for fixed effects, and the accuracy of the method was determined based on the correlation of the ranks of predicted genomic breeding values (GBVs) in both models with the corrected phenotypic values. The analysis was repeated with a subset of SNP markers with largest absolute effects. The results were in agreement with the GBV prediction and the estimation of marker effects for both models for uncensored data and for normality. However, when considering censored data, the Cox model with a normal random effect (S1) was more appropriate. Since there was no agreement between the linear mixed model and the imputed data (L2) for the prediction of genomic values and the estimation of marker effects, the model S1 was considered superior as it took into account the latent variable and the censored data. Marker selection increased correlations between the ranks of predicted GBVs by the linear and Cox frailty models and the corrected phenotypic values, and 120 markers were required to increase the predictive ability for the characteristic analyzed. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-12-02 2015 2018-01-03T23:17:47Z 2018-01-03T23:17:47Z 2018-01-03T23:17:47Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
Genetics and Molecular Research, Ribeirão Preto, v. 14, n. 4, p. 12616-12627, 2015. http://dx.doi.org/10.4238/2015.October.19.5 http://www.alice.cnptia.embrapa.br/alice/handle/doc/1030248 |
identifier_str_mv |
Genetics and Molecular Research, Ribeirão Preto, v. 14, n. 4, p. 12616-12627, 2015. |
url |
http://dx.doi.org/10.4238/2015.October.19.5 http://www.alice.cnptia.embrapa.br/alice/handle/doc/1030248 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa) instacron:EMBRAPA |
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Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
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EMBRAPA |
institution |
EMBRAPA |
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Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
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Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
repository.name.fl_str_mv |
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
repository.mail.fl_str_mv |
cg-riaa@embrapa.br |
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1794503447207215104 |