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fullfact: an R package for the analysis of genetic and maternal variance components from full factorial mating designs

Full factorial breeding designs are useful for quantifying the amount of additive genetic, nonadditive genetic, and maternal variance that explain phenotypic traits. Such variance estimates are important for examining evolutionary potential. Traditionally, full factorial mating designs have been ana...

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Autores principales: Houde, Aimee Lee S., Pitcher, Trevor E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752957/
https://www.ncbi.nlm.nih.gov/pubmed/26909144
http://dx.doi.org/10.1002/ece3.1943
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author Houde, Aimee Lee S.
Pitcher, Trevor E.
author_facet Houde, Aimee Lee S.
Pitcher, Trevor E.
author_sort Houde, Aimee Lee S.
collection PubMed
description Full factorial breeding designs are useful for quantifying the amount of additive genetic, nonadditive genetic, and maternal variance that explain phenotypic traits. Such variance estimates are important for examining evolutionary potential. Traditionally, full factorial mating designs have been analyzed using a two‐way analysis of variance, which may produce negative variance values and is not suited for unbalanced designs. Mixed‐effects models do not produce negative variance values and are suited for unbalanced designs. However, extracting the variance components, calculating significance values, and estimating confidence intervals and/or power values for the components are not straightforward using traditional analytic methods. We introduce fullfact – an R package that addresses these issues and facilitates the analysis of full factorial mating designs with mixed‐effects models. Here, we summarize the functions of the fullfact package. The observed data functions extract the variance explained by random and fixed effects and provide their significance. We then calculate the additive genetic, nonadditive genetic, and maternal variance components explaining the phenotype. In particular, we integrate nonnormal error structures for estimating these components for nonnormal data types. The resampled data functions are used to produce bootstrap‐t confidence intervals, which can then be plotted using a simple function. We explore the fullfact package through a worked example. This package will facilitate the analyses of full factorial mating designs in R, especially for the analysis of binary, proportion, and/or count data types and for the ability to incorporate additional random and fixed effects and power analyses.
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spelling pubmed-47529572016-02-23 fullfact: an R package for the analysis of genetic and maternal variance components from full factorial mating designs Houde, Aimee Lee S. Pitcher, Trevor E. Ecol Evol Original Research Full factorial breeding designs are useful for quantifying the amount of additive genetic, nonadditive genetic, and maternal variance that explain phenotypic traits. Such variance estimates are important for examining evolutionary potential. Traditionally, full factorial mating designs have been analyzed using a two‐way analysis of variance, which may produce negative variance values and is not suited for unbalanced designs. Mixed‐effects models do not produce negative variance values and are suited for unbalanced designs. However, extracting the variance components, calculating significance values, and estimating confidence intervals and/or power values for the components are not straightforward using traditional analytic methods. We introduce fullfact – an R package that addresses these issues and facilitates the analysis of full factorial mating designs with mixed‐effects models. Here, we summarize the functions of the fullfact package. The observed data functions extract the variance explained by random and fixed effects and provide their significance. We then calculate the additive genetic, nonadditive genetic, and maternal variance components explaining the phenotype. In particular, we integrate nonnormal error structures for estimating these components for nonnormal data types. The resampled data functions are used to produce bootstrap‐t confidence intervals, which can then be plotted using a simple function. We explore the fullfact package through a worked example. This package will facilitate the analyses of full factorial mating designs in R, especially for the analysis of binary, proportion, and/or count data types and for the ability to incorporate additional random and fixed effects and power analyses. John Wiley and Sons Inc. 2016-02-14 /pmc/articles/PMC4752957/ /pubmed/26909144 http://dx.doi.org/10.1002/ece3.1943 Text en © 2016 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Houde, Aimee Lee S.
Pitcher, Trevor E.
fullfact: an R package for the analysis of genetic and maternal variance components from full factorial mating designs
title fullfact: an R package for the analysis of genetic and maternal variance components from full factorial mating designs
title_full fullfact: an R package for the analysis of genetic and maternal variance components from full factorial mating designs
title_fullStr fullfact: an R package for the analysis of genetic and maternal variance components from full factorial mating designs
title_full_unstemmed fullfact: an R package for the analysis of genetic and maternal variance components from full factorial mating designs
title_short fullfact: an R package for the analysis of genetic and maternal variance components from full factorial mating designs
title_sort fullfact: an r package for the analysis of genetic and maternal variance components from full factorial mating designs
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752957/
https://www.ncbi.nlm.nih.gov/pubmed/26909144
http://dx.doi.org/10.1002/ece3.1943
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