Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection

Detalhes bibliográficos
Autor(a) principal: Pimentel,Eduardo da Cruz Gouveia
Data de Publicação: 2010
Outros Autores: Sargolzaei,Mehdi, Simianer,Henner, Schenkel,Flávio Schramm, Liu,Zengting, Fries,Luiz Alberto, Queiroz,Sandra Aidar de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Genetics and Molecular Biology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100033
Resumo: The aim of this study was to compare iterative and direct solvers for estimation of marker effects in genomic selection. One iterative and two direct methods were used: Gauss-Seidel with Residual Update, Cholesky Decomposition and Gentleman-Givens rotations. For resembling different scenarios with respect to number of markers and of genotyped animals, a simulated data set divided into 25 subsets was used. Number of markers ranged from 1,200 to 5,925 and number of animals ranged from 1,200 to 5,865. Methods were also applied to real data comprising 3081 individuals genotyped for 45181 SNPs. Results from simulated data showed that the iterative solver was substantially faster than direct methods for larger numbers of markers. Use of a direct solver may allow for computing (co)variances of SNP effects. When applied to real data, performance of the iterative method varied substantially, depending on the level of ill-conditioning of the coefficient matrix. From results with real data, Gentleman-Givens rotations would be the method of choice in this particular application as it provided an exact solution within a fairly reasonable time frame (less than two hours). It would indeed be the preferred method whenever computer resources allow its use.
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spelling Use of direct and iterative solvers for estimation of SNP effects in genome-wide selectionbreeding valuegenomic selectionmixed model equationsnumerical methodThe aim of this study was to compare iterative and direct solvers for estimation of marker effects in genomic selection. One iterative and two direct methods were used: Gauss-Seidel with Residual Update, Cholesky Decomposition and Gentleman-Givens rotations. For resembling different scenarios with respect to number of markers and of genotyped animals, a simulated data set divided into 25 subsets was used. Number of markers ranged from 1,200 to 5,925 and number of animals ranged from 1,200 to 5,865. Methods were also applied to real data comprising 3081 individuals genotyped for 45181 SNPs. Results from simulated data showed that the iterative solver was substantially faster than direct methods for larger numbers of markers. Use of a direct solver may allow for computing (co)variances of SNP effects. When applied to real data, performance of the iterative method varied substantially, depending on the level of ill-conditioning of the coefficient matrix. From results with real data, Gentleman-Givens rotations would be the method of choice in this particular application as it provided an exact solution within a fairly reasonable time frame (less than two hours). It would indeed be the preferred method whenever computer resources allow its use.Sociedade Brasileira de Genética2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100033Genetics and Molecular Biology v.33 n.1 2010reponame:Genetics and Molecular Biologyinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/S1415-47572010005000014info:eu-repo/semantics/openAccessPimentel,Eduardo da Cruz GouveiaSargolzaei,MehdiSimianer,HennerSchenkel,Flávio SchrammLiu,ZengtingFries,Luiz AlbertoQueiroz,Sandra Aidar deeng2010-02-12T00:00:00Zoai:scielo:S1415-47572010000100033Revistahttp://www.gmb.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||editor@gmb.org.br1678-46851415-4757opendoar:2010-02-12T00:00Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)false
dc.title.none.fl_str_mv Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection
title Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection
spellingShingle Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection
Pimentel,Eduardo da Cruz Gouveia
breeding value
genomic selection
mixed model equations
numerical method
title_short Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection
title_full Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection
title_fullStr Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection
title_full_unstemmed Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection
title_sort Use of direct and iterative solvers for estimation of SNP effects in genome-wide selection
author Pimentel,Eduardo da Cruz Gouveia
author_facet Pimentel,Eduardo da Cruz Gouveia
Sargolzaei,Mehdi
Simianer,Henner
Schenkel,Flávio Schramm
Liu,Zengting
Fries,Luiz Alberto
Queiroz,Sandra Aidar de
author_role author
author2 Sargolzaei,Mehdi
Simianer,Henner
Schenkel,Flávio Schramm
Liu,Zengting
Fries,Luiz Alberto
Queiroz,Sandra Aidar de
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Pimentel,Eduardo da Cruz Gouveia
Sargolzaei,Mehdi
Simianer,Henner
Schenkel,Flávio Schramm
Liu,Zengting
Fries,Luiz Alberto
Queiroz,Sandra Aidar de
dc.subject.por.fl_str_mv breeding value
genomic selection
mixed model equations
numerical method
topic breeding value
genomic selection
mixed model equations
numerical method
description The aim of this study was to compare iterative and direct solvers for estimation of marker effects in genomic selection. One iterative and two direct methods were used: Gauss-Seidel with Residual Update, Cholesky Decomposition and Gentleman-Givens rotations. For resembling different scenarios with respect to number of markers and of genotyped animals, a simulated data set divided into 25 subsets was used. Number of markers ranged from 1,200 to 5,925 and number of animals ranged from 1,200 to 5,865. Methods were also applied to real data comprising 3081 individuals genotyped for 45181 SNPs. Results from simulated data showed that the iterative solver was substantially faster than direct methods for larger numbers of markers. Use of a direct solver may allow for computing (co)variances of SNP effects. When applied to real data, performance of the iterative method varied substantially, depending on the level of ill-conditioning of the coefficient matrix. From results with real data, Gentleman-Givens rotations would be the method of choice in this particular application as it provided an exact solution within a fairly reasonable time frame (less than two hours). It would indeed be the preferred method whenever computer resources allow its use.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100033
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100033
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1415-47572010005000014
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Genética
publisher.none.fl_str_mv Sociedade Brasileira de Genética
dc.source.none.fl_str_mv Genetics and Molecular Biology v.33 n.1 2010
reponame:Genetics and Molecular Biology
instname:Sociedade Brasileira de Genética (SBG)
instacron:SBG
instname_str Sociedade Brasileira de Genética (SBG)
instacron_str SBG
institution SBG
reponame_str Genetics and Molecular Biology
collection Genetics and Molecular Biology
repository.name.fl_str_mv Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)
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