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Comparison of analyses of the QTLMAS XIV common dataset. I: genomic selection
BACKGROUND: For the XIV QTLMAS workshop, a dataset for traits with complex genetic architecture has been simulated and released for analyses by participants. One of the tasks was to estimate direct genomic values for individuals without phenotypes. The aim of this paper was to compare results of dif...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103194/ https://www.ncbi.nlm.nih.gov/pubmed/21624165 http://dx.doi.org/10.1186/1753-6561-5-S3-S1 |
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author | Pszczola, Marcin Strabel, Tomasz Wolc, Anna Mucha, Sebastian Szydlowski, Maciej |
author_facet | Pszczola, Marcin Strabel, Tomasz Wolc, Anna Mucha, Sebastian Szydlowski, Maciej |
author_sort | Pszczola, Marcin |
collection | PubMed |
description | BACKGROUND: For the XIV QTLMAS workshop, a dataset for traits with complex genetic architecture has been simulated and released for analyses by participants. One of the tasks was to estimate direct genomic values for individuals without phenotypes. The aim of this paper was to compare results of different approaches used by the participants to calculate direct genomic values for quantitative trait (QT) and binary trait (BT). RESULTS: Participants applied 26 approaches for QT and 15 approaches for BT. Accuracy for QT was between 0.26 and 0.89 for males and between 0.31 and 0.89 for females, and for BT ranged from 0.27 to 0.85. For QT, percentage of lost response to selection varied from 8% to 83%, whereas for BT the loss was between 15% and 71%. CONCLUSIONS: Bayesian model averaging methods predicted breeding values slightly better than GBLUP in a simulated data set. The methods utilizing genomic information performed better than traditional pedigree based BLUP analyses. Bivariate analyses was slightly advantageous over single trait for the same method. None of the methods estimated the non-additivity of QTL affecting the QT, which may be one of the constrains in accuracy observed in real data. |
format | Text |
id | pubmed-3103194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31031942011-05-28 Comparison of analyses of the QTLMAS XIV common dataset. I: genomic selection Pszczola, Marcin Strabel, Tomasz Wolc, Anna Mucha, Sebastian Szydlowski, Maciej BMC Proc Proceedings BACKGROUND: For the XIV QTLMAS workshop, a dataset for traits with complex genetic architecture has been simulated and released for analyses by participants. One of the tasks was to estimate direct genomic values for individuals without phenotypes. The aim of this paper was to compare results of different approaches used by the participants to calculate direct genomic values for quantitative trait (QT) and binary trait (BT). RESULTS: Participants applied 26 approaches for QT and 15 approaches for BT. Accuracy for QT was between 0.26 and 0.89 for males and between 0.31 and 0.89 for females, and for BT ranged from 0.27 to 0.85. For QT, percentage of lost response to selection varied from 8% to 83%, whereas for BT the loss was between 15% and 71%. CONCLUSIONS: Bayesian model averaging methods predicted breeding values slightly better than GBLUP in a simulated data set. The methods utilizing genomic information performed better than traditional pedigree based BLUP analyses. Bivariate analyses was slightly advantageous over single trait for the same method. None of the methods estimated the non-additivity of QTL affecting the QT, which may be one of the constrains in accuracy observed in real data. BioMed Central 2011-05-27 /pmc/articles/PMC3103194/ /pubmed/21624165 http://dx.doi.org/10.1186/1753-6561-5-S3-S1 Text en Copyright ©2011 Pszczola 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 Pszczola, Marcin Strabel, Tomasz Wolc, Anna Mucha, Sebastian Szydlowski, Maciej Comparison of analyses of the QTLMAS XIV common dataset. I: genomic selection |
title | Comparison of analyses of the QTLMAS XIV common dataset. I: genomic selection |
title_full | Comparison of analyses of the QTLMAS XIV common dataset. I: genomic selection |
title_fullStr | Comparison of analyses of the QTLMAS XIV common dataset. I: genomic selection |
title_full_unstemmed | Comparison of analyses of the QTLMAS XIV common dataset. I: genomic selection |
title_short | Comparison of analyses of the QTLMAS XIV common dataset. I: genomic selection |
title_sort | comparison of analyses of the qtlmas xiv common dataset. i: genomic selection |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103194/ https://www.ncbi.nlm.nih.gov/pubmed/21624165 http://dx.doi.org/10.1186/1753-6561-5-S3-S1 |
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