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Mendelian sampling covariability of marker effects and genetic values
BACKGROUND: Measures of the expected genetic variability among full-sibs are of practical relevance, such as in the context of mating decisions. An important application field in animal and plant breeding is the selection and allocation of mates when large or small amounts of genetic variability amo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842306/ https://www.ncbi.nlm.nih.gov/pubmed/27107720 http://dx.doi.org/10.1186/s12711-016-0214-0 |
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author | Bonk, Sarah Reichelt, Manuela Teuscher, Friedrich Segelke, Dierck Reinsch, Norbert |
author_facet | Bonk, Sarah Reichelt, Manuela Teuscher, Friedrich Segelke, Dierck Reinsch, Norbert |
author_sort | Bonk, Sarah |
collection | PubMed |
description | BACKGROUND: Measures of the expected genetic variability among full-sibs are of practical relevance, such as in the context of mating decisions. An important application field in animal and plant breeding is the selection and allocation of mates when large or small amounts of genetic variability among offspring are desired, depending on user-specific goals. Estimates of the Mendelian sampling variance can be obtained by simulating gametes from parents with known diplotypes. Knowledge of recombination rates and additive marker effects is also required. In this study, we aimed at developing an exact method that can account for both additive and dominance effects. RESULTS: We derived parent-specific covariance matrices that exactly quantify the within-family (co-)variability of additive and dominance marker effects. These matrices incorporate prior knowledge of the parental diplotypes and recombination rates. When combined with additive marker effects, they allow the exact derivation of the Mendelian sampling (co-)variances of (estimated) breeding values for several traits, as well for the aggregate genotype. A comparative analysis demonstrated good average agreement between the exact values and the simulation results for a practical dataset (74,353 German Holstein cattle). CONCLUSIONS: The newly derived method is suitable for calculating the exact amount of intra-family variation of the estimated breeding values and genetic values (comprising additive and dominance effects). |
format | Online Article Text |
id | pubmed-4842306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48423062016-04-25 Mendelian sampling covariability of marker effects and genetic values Bonk, Sarah Reichelt, Manuela Teuscher, Friedrich Segelke, Dierck Reinsch, Norbert Genet Sel Evol Research Article BACKGROUND: Measures of the expected genetic variability among full-sibs are of practical relevance, such as in the context of mating decisions. An important application field in animal and plant breeding is the selection and allocation of mates when large or small amounts of genetic variability among offspring are desired, depending on user-specific goals. Estimates of the Mendelian sampling variance can be obtained by simulating gametes from parents with known diplotypes. Knowledge of recombination rates and additive marker effects is also required. In this study, we aimed at developing an exact method that can account for both additive and dominance effects. RESULTS: We derived parent-specific covariance matrices that exactly quantify the within-family (co-)variability of additive and dominance marker effects. These matrices incorporate prior knowledge of the parental diplotypes and recombination rates. When combined with additive marker effects, they allow the exact derivation of the Mendelian sampling (co-)variances of (estimated) breeding values for several traits, as well for the aggregate genotype. A comparative analysis demonstrated good average agreement between the exact values and the simulation results for a practical dataset (74,353 German Holstein cattle). CONCLUSIONS: The newly derived method is suitable for calculating the exact amount of intra-family variation of the estimated breeding values and genetic values (comprising additive and dominance effects). BioMed Central 2016-04-23 /pmc/articles/PMC4842306/ /pubmed/27107720 http://dx.doi.org/10.1186/s12711-016-0214-0 Text en © Bonk et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Bonk, Sarah Reichelt, Manuela Teuscher, Friedrich Segelke, Dierck Reinsch, Norbert Mendelian sampling covariability of marker effects and genetic values |
title | Mendelian sampling covariability of marker effects and genetic values |
title_full | Mendelian sampling covariability of marker effects and genetic values |
title_fullStr | Mendelian sampling covariability of marker effects and genetic values |
title_full_unstemmed | Mendelian sampling covariability of marker effects and genetic values |
title_short | Mendelian sampling covariability of marker effects and genetic values |
title_sort | mendelian sampling covariability of marker effects and genetic values |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842306/ https://www.ncbi.nlm.nih.gov/pubmed/27107720 http://dx.doi.org/10.1186/s12711-016-0214-0 |
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