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A simple algorithm to estimate genetic variance in an animal threshold model using Bayesian inference

BACKGROUND: In the genetic analysis of binary traits with one observation per animal, animal threshold models frequently give biased heritability estimates. In some cases, this problem can be circumvented by fitting sire- or sire-dam models. However, these models are not appropriate in cases where i...

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Detalles Bibliográficos
Autores principales: Ødegård, Jørgen, Meuwissen, Theo HE, Heringstad, Bjørg, Madsen, Per
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2918534/
https://www.ncbi.nlm.nih.gov/pubmed/20649962
http://dx.doi.org/10.1186/1297-9686-42-29
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author Ødegård, Jørgen
Meuwissen, Theo HE
Heringstad, Bjørg
Madsen, Per
author_facet Ødegård, Jørgen
Meuwissen, Theo HE
Heringstad, Bjørg
Madsen, Per
author_sort Ødegård, Jørgen
collection PubMed
description BACKGROUND: In the genetic analysis of binary traits with one observation per animal, animal threshold models frequently give biased heritability estimates. In some cases, this problem can be circumvented by fitting sire- or sire-dam models. However, these models are not appropriate in cases where individual records exist on parents. Therefore, the aim of our study was to develop a new Gibbs sampling algorithm for a proper estimation of genetic (co)variance components within an animal threshold model framework. METHODS: In the proposed algorithm, individuals are classified as either "informative" or "non-informative" with respect to genetic (co)variance components. The "non-informative" individuals are characterized by their Mendelian sampling deviations (deviance from the mid-parent mean) being completely confounded with a single residual on the underlying liability scale. For threshold models, residual variance on the underlying scale is not identifiable. Hence, variance of fully confounded Mendelian sampling deviations cannot be identified either, but can be inferred from the between-family variation. In the new algorithm, breeding values are sampled as in a standard animal model using the full relationship matrix, but genetic (co)variance components are inferred from the sampled breeding values and relationships between "informative" individuals (usually parents) only. The latter is analogous to a sire-dam model (in cases with no individual records on the parents). RESULTS: When applied to simulated data sets, the standard animal threshold model failed to produce useful results since samples of genetic variance always drifted towards infinity, while the new algorithm produced proper parameter estimates essentially identical to the results from a sire-dam model (given the fact that no individual records exist for the parents). Furthermore, the new algorithm showed much faster Markov chain mixing properties for genetic parameters (similar to the sire-dam model). CONCLUSIONS: The new algorithm to estimate genetic parameters via Gibbs sampling solves the bias problems typically occurring in animal threshold model analysis of binary traits with one observation per animal. Furthermore, the method considerably speeds up mixing properties of the Gibbs sampler with respect to genetic parameters, which would be an advantage of any linear or non-linear animal model.
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spelling pubmed-29185342010-08-10 A simple algorithm to estimate genetic variance in an animal threshold model using Bayesian inference Ødegård, Jørgen Meuwissen, Theo HE Heringstad, Bjørg Madsen, Per Genet Sel Evol Research BACKGROUND: In the genetic analysis of binary traits with one observation per animal, animal threshold models frequently give biased heritability estimates. In some cases, this problem can be circumvented by fitting sire- or sire-dam models. However, these models are not appropriate in cases where individual records exist on parents. Therefore, the aim of our study was to develop a new Gibbs sampling algorithm for a proper estimation of genetic (co)variance components within an animal threshold model framework. METHODS: In the proposed algorithm, individuals are classified as either "informative" or "non-informative" with respect to genetic (co)variance components. The "non-informative" individuals are characterized by their Mendelian sampling deviations (deviance from the mid-parent mean) being completely confounded with a single residual on the underlying liability scale. For threshold models, residual variance on the underlying scale is not identifiable. Hence, variance of fully confounded Mendelian sampling deviations cannot be identified either, but can be inferred from the between-family variation. In the new algorithm, breeding values are sampled as in a standard animal model using the full relationship matrix, but genetic (co)variance components are inferred from the sampled breeding values and relationships between "informative" individuals (usually parents) only. The latter is analogous to a sire-dam model (in cases with no individual records on the parents). RESULTS: When applied to simulated data sets, the standard animal threshold model failed to produce useful results since samples of genetic variance always drifted towards infinity, while the new algorithm produced proper parameter estimates essentially identical to the results from a sire-dam model (given the fact that no individual records exist for the parents). Furthermore, the new algorithm showed much faster Markov chain mixing properties for genetic parameters (similar to the sire-dam model). CONCLUSIONS: The new algorithm to estimate genetic parameters via Gibbs sampling solves the bias problems typically occurring in animal threshold model analysis of binary traits with one observation per animal. Furthermore, the method considerably speeds up mixing properties of the Gibbs sampler with respect to genetic parameters, which would be an advantage of any linear or non-linear animal model. BioMed Central 2010-07-22 /pmc/articles/PMC2918534/ /pubmed/20649962 http://dx.doi.org/10.1186/1297-9686-42-29 Text en Copyright ©2010 Ødegård et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Ødegård, Jørgen
Meuwissen, Theo HE
Heringstad, Bjørg
Madsen, Per
A simple algorithm to estimate genetic variance in an animal threshold model using Bayesian inference
title A simple algorithm to estimate genetic variance in an animal threshold model using Bayesian inference
title_full A simple algorithm to estimate genetic variance in an animal threshold model using Bayesian inference
title_fullStr A simple algorithm to estimate genetic variance in an animal threshold model using Bayesian inference
title_full_unstemmed A simple algorithm to estimate genetic variance in an animal threshold model using Bayesian inference
title_short A simple algorithm to estimate genetic variance in an animal threshold model using Bayesian inference
title_sort simple algorithm to estimate genetic variance in an animal threshold model using bayesian inference
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2918534/
https://www.ncbi.nlm.nih.gov/pubmed/20649962
http://dx.doi.org/10.1186/1297-9686-42-29
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