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Comparison of the analyses of the XV(th )QTLMAS common dataset II: QTL analysis

BACKGROUND: The QTLMAS XV(th )dataset consisted of the pedigrees, marker genotypes and quantitative trait performances of 2,000 phenotyped animals with a half-sib family structure. The trait was regulated by 8 QTL which display additive, imprinting or epistatic effects. This paper aims at comparing...

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Autores principales: Demeure, Olivier, Filangi, Olivier, Elsen, Jean-Michel, Le Roy, Pascale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3363156/
https://www.ncbi.nlm.nih.gov/pubmed/22640591
http://dx.doi.org/10.1186/1753-6561-6-S2-S2
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author Demeure, Olivier
Filangi, Olivier
Elsen, Jean-Michel
Le Roy, Pascale
author_facet Demeure, Olivier
Filangi, Olivier
Elsen, Jean-Michel
Le Roy, Pascale
author_sort Demeure, Olivier
collection PubMed
description BACKGROUND: The QTLMAS XV(th )dataset consisted of the pedigrees, marker genotypes and quantitative trait performances of 2,000 phenotyped animals with a half-sib family structure. The trait was regulated by 8 QTL which display additive, imprinting or epistatic effects. This paper aims at comparing the QTL mapping results obtained by six participants of the workshop. METHODS: Different regression, GBLUP, LASSO and Bayesian methods were applied for QTL detection. The results of these methods are compared based on the number of correctly mapped QTL, the number of false positives, the accuracy of the QTL location and the estimation of the QTL effect. RESULTS: All the simulated QTL, except the interacting QTL on Chr5, were identified by the participants. Depending on the method, 3 to 7 out of the 8 QTL were identified. The distance to the real location and the accuracy of the QTL effect varied to a large extent depending on the methods and complexity of the simulated QTL. CONCLUSIONS: While all methods were fairly efficient in detecting QTL with additive effects, it was clear that for non-additive situations, such as parent-of-origin effects or interactions, the BayesC method gave the best results by detecting 7 out of the 8 simulated QTL, with only two false positives and a good precision (less than 1 cM away on average). Indeed, if LASSO could detect QTL even in complex situations, it was associated with too many false positive results to allow for efficient GWAS. GENMIX, a method based on the phylogenies of local haplotypes, also appeared as a promising approach, which however showed a few more false positives when compared with the BayesC method.
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spelling pubmed-33631562012-05-31 Comparison of the analyses of the XV(th )QTLMAS common dataset II: QTL analysis Demeure, Olivier Filangi, Olivier Elsen, Jean-Michel Le Roy, Pascale BMC Proc Proceedings BACKGROUND: The QTLMAS XV(th )dataset consisted of the pedigrees, marker genotypes and quantitative trait performances of 2,000 phenotyped animals with a half-sib family structure. The trait was regulated by 8 QTL which display additive, imprinting or epistatic effects. This paper aims at comparing the QTL mapping results obtained by six participants of the workshop. METHODS: Different regression, GBLUP, LASSO and Bayesian methods were applied for QTL detection. The results of these methods are compared based on the number of correctly mapped QTL, the number of false positives, the accuracy of the QTL location and the estimation of the QTL effect. RESULTS: All the simulated QTL, except the interacting QTL on Chr5, were identified by the participants. Depending on the method, 3 to 7 out of the 8 QTL were identified. The distance to the real location and the accuracy of the QTL effect varied to a large extent depending on the methods and complexity of the simulated QTL. CONCLUSIONS: While all methods were fairly efficient in detecting QTL with additive effects, it was clear that for non-additive situations, such as parent-of-origin effects or interactions, the BayesC method gave the best results by detecting 7 out of the 8 simulated QTL, with only two false positives and a good precision (less than 1 cM away on average). Indeed, if LASSO could detect QTL even in complex situations, it was associated with too many false positive results to allow for efficient GWAS. GENMIX, a method based on the phylogenies of local haplotypes, also appeared as a promising approach, which however showed a few more false positives when compared with the BayesC method. BioMed Central 2012-05-21 /pmc/articles/PMC3363156/ /pubmed/22640591 http://dx.doi.org/10.1186/1753-6561-6-S2-S2 Text en Copyright ©2012 Demeure 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
Demeure, Olivier
Filangi, Olivier
Elsen, Jean-Michel
Le Roy, Pascale
Comparison of the analyses of the XV(th )QTLMAS common dataset II: QTL analysis
title Comparison of the analyses of the XV(th )QTLMAS common dataset II: QTL analysis
title_full Comparison of the analyses of the XV(th )QTLMAS common dataset II: QTL analysis
title_fullStr Comparison of the analyses of the XV(th )QTLMAS common dataset II: QTL analysis
title_full_unstemmed Comparison of the analyses of the XV(th )QTLMAS common dataset II: QTL analysis
title_short Comparison of the analyses of the XV(th )QTLMAS common dataset II: QTL analysis
title_sort comparison of the analyses of the xv(th )qtlmas common dataset ii: qtl analysis
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3363156/
https://www.ncbi.nlm.nih.gov/pubmed/22640591
http://dx.doi.org/10.1186/1753-6561-6-S2-S2
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