Hierarchical Spatial Process Models for Multiple Traits in Large Genetic Trials

This article expands upon recent interest in Bayesian hierarchical models in quantitative genetics by developing spatial process models for inference on additive and dominance genetic variance within the context of large spatially referenced trial datasets of multiple traits of interest. Direct appl...

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Published in:Journal of the American Statistical Association
Main Authors: Banerjee, Sudipto, Finley, Andrew O., Waldmann, Patrik, Ericsson, Tore
Format: Text
Language:English
Published: 2010
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911798
http://www.ncbi.nlm.nih.gov/pubmed/20676229
https://doi.org/10.1198/jasa.2009.ap09068
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spelling ftpubmed:oai:pubmedcentral.nih.gov:2911798 2023-05-15T17:44:50+02:00 Hierarchical Spatial Process Models for Multiple Traits in Large Genetic Trials Banerjee, Sudipto Finley, Andrew O. Waldmann, Patrik Ericsson, Tore 2010-06-01 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911798 http://www.ncbi.nlm.nih.gov/pubmed/20676229 https://doi.org/10.1198/jasa.2009.ap09068 en eng http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911798 http://www.ncbi.nlm.nih.gov/pubmed/20676229 http://dx.doi.org/10.1198/jasa.2009.ap09068 Article Text 2010 ftpubmed https://doi.org/10.1198/jasa.2009.ap09068 2013-09-03T03:07:20Z This article expands upon recent interest in Bayesian hierarchical models in quantitative genetics by developing spatial process models for inference on additive and dominance genetic variance within the context of large spatially referenced trial datasets of multiple traits of interest. Direct application of such multivariate models to large spatial datasets is often computationally infeasible because of cubic order matrix algorithms involved in estimation. The situation is even worse in Markov chain Monte Carlo (MCMC) contexts where such computations are performed for several thousand iterations. Here, we discuss approaches that help obviate these hurdles without sacrificing the richness in modeling. For genetic effects, we demonstrate how an initial spectral decomposition of the relationship matrices negates the expensive matrix inversions required in previously proposed MCMC methods. For spatial effects we discuss a multivariate predictive process that reduces the computational burden by projecting the original process onto a subspace generated by realizations of the original process at a specified set of locations (or knots). We illustrate the proposed methods using a synthetic dataset with multivariate additive and dominant genetic effects and anisotropic spatial residuals, and a large dataset from a scots pine (Pinus sylvestris L.) progeny study conducted in northern Sweden. Our approaches enable us to provide a comprehensive analysis of this large trial which amply demonstrates that, in addition to violating basic assumptions of the linear model, ignoring spatial effects can result in downwardly biased measures of heritability. Text Northern Sweden PubMed Central (PMC) Journal of the American Statistical Association 105 490 506 521
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Article
spellingShingle Article
Banerjee, Sudipto
Finley, Andrew O.
Waldmann, Patrik
Ericsson, Tore
Hierarchical Spatial Process Models for Multiple Traits in Large Genetic Trials
topic_facet Article
description This article expands upon recent interest in Bayesian hierarchical models in quantitative genetics by developing spatial process models for inference on additive and dominance genetic variance within the context of large spatially referenced trial datasets of multiple traits of interest. Direct application of such multivariate models to large spatial datasets is often computationally infeasible because of cubic order matrix algorithms involved in estimation. The situation is even worse in Markov chain Monte Carlo (MCMC) contexts where such computations are performed for several thousand iterations. Here, we discuss approaches that help obviate these hurdles without sacrificing the richness in modeling. For genetic effects, we demonstrate how an initial spectral decomposition of the relationship matrices negates the expensive matrix inversions required in previously proposed MCMC methods. For spatial effects we discuss a multivariate predictive process that reduces the computational burden by projecting the original process onto a subspace generated by realizations of the original process at a specified set of locations (or knots). We illustrate the proposed methods using a synthetic dataset with multivariate additive and dominant genetic effects and anisotropic spatial residuals, and a large dataset from a scots pine (Pinus sylvestris L.) progeny study conducted in northern Sweden. Our approaches enable us to provide a comprehensive analysis of this large trial which amply demonstrates that, in addition to violating basic assumptions of the linear model, ignoring spatial effects can result in downwardly biased measures of heritability.
format Text
author Banerjee, Sudipto
Finley, Andrew O.
Waldmann, Patrik
Ericsson, Tore
author_facet Banerjee, Sudipto
Finley, Andrew O.
Waldmann, Patrik
Ericsson, Tore
author_sort Banerjee, Sudipto
title Hierarchical Spatial Process Models for Multiple Traits in Large Genetic Trials
title_short Hierarchical Spatial Process Models for Multiple Traits in Large Genetic Trials
title_full Hierarchical Spatial Process Models for Multiple Traits in Large Genetic Trials
title_fullStr Hierarchical Spatial Process Models for Multiple Traits in Large Genetic Trials
title_full_unstemmed Hierarchical Spatial Process Models for Multiple Traits in Large Genetic Trials
title_sort hierarchical spatial process models for multiple traits in large genetic trials
publishDate 2010
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911798
http://www.ncbi.nlm.nih.gov/pubmed/20676229
https://doi.org/10.1198/jasa.2009.ap09068
genre Northern Sweden
genre_facet Northern Sweden
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911798
http://www.ncbi.nlm.nih.gov/pubmed/20676229
http://dx.doi.org/10.1198/jasa.2009.ap09068
op_doi https://doi.org/10.1198/jasa.2009.ap09068
container_title Journal of the American Statistical Association
container_volume 105
container_issue 490
container_start_page 506
op_container_end_page 521
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