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Bayesian shrinkage mapping of quantitative trait loci in variance component models

BACKGROUND: In this article, I propose a model-selection-free method to map multiple quantitative trait loci (QTL) in variance component model, which is useful in outbred populations. The new method can estimate the variance of zero-effect QTL infinitely to zero, but nearly unbiased for non-zero-eff...

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Detalles Bibliográficos
Autor principal: Fang, Ming
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874758/
https://www.ncbi.nlm.nih.gov/pubmed/20429900
http://dx.doi.org/10.1186/1471-2156-11-30
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author Fang, Ming
author_facet Fang, Ming
author_sort Fang, Ming
collection PubMed
description BACKGROUND: In this article, I propose a model-selection-free method to map multiple quantitative trait loci (QTL) in variance component model, which is useful in outbred populations. The new method can estimate the variance of zero-effect QTL infinitely to zero, but nearly unbiased for non-zero-effect QTL. It is analogous to Xu's Bayesian shrinkage estimation method, but his method is based on allelic substitution model, while the new method is based on the variance component models. RESULTS: Extensive simulation experiments were conducted to investigate the performance of the proposed method. The results showed that the proposed method was efficient in mapping multiple QTL simultaneously, and moreover it was more competitive than the reversible jump MCMC (RJMCMC) method and may even out-perform it. CONCLUSIONS: The newly developed Bayesian shrinkage method is very efficient and powerful for mapping multiple QTL in outbred populations.
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spelling pubmed-28747582010-05-24 Bayesian shrinkage mapping of quantitative trait loci in variance component models Fang, Ming BMC Genet Methodology article BACKGROUND: In this article, I propose a model-selection-free method to map multiple quantitative trait loci (QTL) in variance component model, which is useful in outbred populations. The new method can estimate the variance of zero-effect QTL infinitely to zero, but nearly unbiased for non-zero-effect QTL. It is analogous to Xu's Bayesian shrinkage estimation method, but his method is based on allelic substitution model, while the new method is based on the variance component models. RESULTS: Extensive simulation experiments were conducted to investigate the performance of the proposed method. The results showed that the proposed method was efficient in mapping multiple QTL simultaneously, and moreover it was more competitive than the reversible jump MCMC (RJMCMC) method and may even out-perform it. CONCLUSIONS: The newly developed Bayesian shrinkage method is very efficient and powerful for mapping multiple QTL in outbred populations. BioMed Central 2010-04-29 /pmc/articles/PMC2874758/ /pubmed/20429900 http://dx.doi.org/10.1186/1471-2156-11-30 Text en Copyright ©2010 Fang; 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 Methodology article
Fang, Ming
Bayesian shrinkage mapping of quantitative trait loci in variance component models
title Bayesian shrinkage mapping of quantitative trait loci in variance component models
title_full Bayesian shrinkage mapping of quantitative trait loci in variance component models
title_fullStr Bayesian shrinkage mapping of quantitative trait loci in variance component models
title_full_unstemmed Bayesian shrinkage mapping of quantitative trait loci in variance component models
title_short Bayesian shrinkage mapping of quantitative trait loci in variance component models
title_sort bayesian shrinkage mapping of quantitative trait loci in variance component models
topic Methodology article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874758/
https://www.ncbi.nlm.nih.gov/pubmed/20429900
http://dx.doi.org/10.1186/1471-2156-11-30
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