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Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps
BACKGROUND: Genome-wide dense markers have been used to detect genes and estimate relative genetic values. Among many methods, Bayesian techniques have been widely used and shown to be powerful in genome-wide breeding value estimation and association studies. However, computation is known to be inte...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103199/ https://www.ncbi.nlm.nih.gov/pubmed/21624170 http://dx.doi.org/10.1186/1753-6561-5-S3-S14 |
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author | Shen, Xia Rönnegård, Lars Carlborg, Örjan |
author_facet | Shen, Xia Rönnegård, Lars Carlborg, Örjan |
author_sort | Shen, Xia |
collection | PubMed |
description | BACKGROUND: Genome-wide dense markers have been used to detect genes and estimate relative genetic values. Among many methods, Bayesian techniques have been widely used and shown to be powerful in genome-wide breeding value estimation and association studies. However, computation is known to be intensive under the Bayesian framework, and specifying a prior distribution for each parameter is always required for Bayesian computation. We propose the use of hierarchical likelihood to solve such problems. RESULTS: Using double hierarchical generalized linear models, we analyzed the simulated dataset provided by the QTLMAS 2010 workshop. Marker-specific variances estimated by double hierarchical generalized linear models identified the QTL with large effects for both the quantitative and binary traits. The QTL positions were detected with very high accuracy. For young individuals without phenotypic records, the true and estimated breeding values had Pearson correlation of 0.60 for the quantitative trait and 0.72 for the binary trait, where the quantitative trait had a more complicated genetic architecture involving imprinting and epistatic QTL. CONCLUSIONS: Hierarchical likelihood enables estimation of marker-specific variances under the likelihoodist framework. Double hierarchical generalized linear models are powerful in localizing major QTL and computationally fast. |
format | Text |
id | pubmed-3103199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31031992011-05-28 Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps Shen, Xia Rönnegård, Lars Carlborg, Örjan BMC Proc Proceedings BACKGROUND: Genome-wide dense markers have been used to detect genes and estimate relative genetic values. Among many methods, Bayesian techniques have been widely used and shown to be powerful in genome-wide breeding value estimation and association studies. However, computation is known to be intensive under the Bayesian framework, and specifying a prior distribution for each parameter is always required for Bayesian computation. We propose the use of hierarchical likelihood to solve such problems. RESULTS: Using double hierarchical generalized linear models, we analyzed the simulated dataset provided by the QTLMAS 2010 workshop. Marker-specific variances estimated by double hierarchical generalized linear models identified the QTL with large effects for both the quantitative and binary traits. The QTL positions were detected with very high accuracy. For young individuals without phenotypic records, the true and estimated breeding values had Pearson correlation of 0.60 for the quantitative trait and 0.72 for the binary trait, where the quantitative trait had a more complicated genetic architecture involving imprinting and epistatic QTL. CONCLUSIONS: Hierarchical likelihood enables estimation of marker-specific variances under the likelihoodist framework. Double hierarchical generalized linear models are powerful in localizing major QTL and computationally fast. BioMed Central 2011-05-27 /pmc/articles/PMC3103199/ /pubmed/21624170 http://dx.doi.org/10.1186/1753-6561-5-S3-S14 Text en Copyright ©2011 Shen 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 | Proceedings Shen, Xia Rönnegård, Lars Carlborg, Örjan Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps |
title | Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps |
title_full | Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps |
title_fullStr | Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps |
title_full_unstemmed | Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps |
title_short | Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps |
title_sort | hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103199/ https://www.ncbi.nlm.nih.gov/pubmed/21624170 http://dx.doi.org/10.1186/1753-6561-5-S3-S14 |
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