Parametric and Nonparametric Statistical Methods for Genomic Selection of Traits with Additive and Epistatic Genetic Architectures

dc.contributor.author Howard, Reka
dc.contributor.author Carriquiry, Alicia
dc.contributor.author Carriquiry, Alicia
dc.contributor.author Beavis, William
dc.contributor.department Statistics
dc.date 2018-02-17T06:14:36.000
dc.date.accessioned 2020-07-02T06:57:19Z
dc.date.available 2020-07-02T06:57:19Z
dc.date.copyright Wed Jan 01 00:00:00 UTC 2014
dc.date.issued 2014-06-01
dc.description.abstract <p>Parametric and nonparametric methods have been developed for purposes of predicting phenotypes. These methods are based on retrospective analyses of empirical data consisting of genotypic and phenotypic scores. Recent reports have indicated that parametric methods are unable to predict phenotypes of traits with known epistatic genetic architectures. Herein, we review parametric methods including least squares regression, ridge regression, Bayesian ridge regression, least absolute shrinkage and selection operator (LASSO), Bayesian LASSO, best linear unbiased prediction (BLUP), Bayes A, Bayes B, Bayes C, and Bayes Cp. We also review nonparametric methods including Nadaraya-Watson estimator, reproducing kernel Hilbert space, support vector machine regression, and neural networks. We assess the relative merits of these 14 methods in terms of accuracy and mean squared error (MSE) using simulated genetic architectures consisting of completely additive or two-way epistatic interactions in an F<sub>2</sub> population derived from crosses of inbred lines. Each simulated genetic architecture explained either 30% or 70% of the phenotypic variability. The greatest impact on estimates of accuracy and MSE was due to genetic architecture. Parametric methods were unable to predict phenotypic values when the underlying genetic architecture was based entirely on epistasis. Parametric methods were slightly better than nonparametric methods for additive genetic architectures. Distinctions among parametric methods for additive genetic architectures were incremental. Heritability, i.e., proportion of phenotypic variability, had the second greatest impact on estimates of accuracy and MSE.</p>
dc.description.comments <p>This article is from <em>G3: Genes, Genomes, Genetics</em> 4 (2014): 1027, doi: <a href="http://dx.doi.org/10.1534/g3.114.010298" target="_blank">10.1534/g3.114.010298</a>. Posted with permission.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/stat_las_pubs/23/
dc.identifier.articleid 1023
dc.identifier.contextkey 7852069
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath stat_las_pubs/23
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/90543
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/stat_las_pubs/23/2014_CarriguiryAL_ParametricNonparametricStatistical.pdf|||Fri Jan 14 22:46:18 UTC 2022
dc.source.uri 10.1534/g3.114.010298
dc.subject.disciplines Agronomy and Crop Sciences
dc.subject.disciplines Statistics and Probability
dc.subject.keywords epistasis
dc.subject.keywords genomic selection
dc.subject.keywords GenPred
dc.subject.keywords nonparametric
dc.subject.keywords parametric
dc.subject.keywords prediction
dc.subject.keywords shared data resources
dc.title Parametric and Nonparametric Statistical Methods for Genomic Selection of Traits with Additive and Epistatic Genetic Architectures
dc.type article
dc.type.genre article
dspace.entity.type Publication
relation.isAuthorOfPublication 6ddd5891-2ad0-4a93-89e5-8c35c28b0de4
relation.isOrgUnitOfPublication 264904d9-9e66-4169-8e11-034e537ddbca
File
Original bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
2014_CarriguiryAL_ParametricNonparametricStatistical.pdf
Size:
1.7 MB
Format:
Adobe Portable Document Format
Description:
Collections