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Modelling time course gene expression data with finite mixtures of linear additive models

Summary: A model class of finite mixtures of linear additive models is presented. The component-specific parameters in the regression models are estimated using regularized likelihood methods. The advantages of the regularization are that (i) the pre-specified maximum degrees of freedom for the spli...

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Autores principales: Grün, Bettina, Scharl, Theresa, Leisch, Friedrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3259441/
https://www.ncbi.nlm.nih.gov/pubmed/22121159
http://dx.doi.org/10.1093/bioinformatics/btr653
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author Grün, Bettina
Scharl, Theresa
Leisch, Friedrich
author_facet Grün, Bettina
Scharl, Theresa
Leisch, Friedrich
author_sort Grün, Bettina
collection PubMed
description Summary: A model class of finite mixtures of linear additive models is presented. The component-specific parameters in the regression models are estimated using regularized likelihood methods. The advantages of the regularization are that (i) the pre-specified maximum degrees of freedom for the splines is less crucial than for unregularized estimation and that (ii) for each component individually a suitable degree of freedom is selected in an automatic way. The performance is evaluated in a simulation study with artificial data as well as on a yeast cell cycle dataset of gene expression levels over time. Availability: The latest release version of the R package flexmix is available from CRAN (http://cran.r-project.org/). Contact: Bettina.Gruen@jku.at
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spelling pubmed-32594412012-01-17 Modelling time course gene expression data with finite mixtures of linear additive models Grün, Bettina Scharl, Theresa Leisch, Friedrich Bioinformatics Original Papers Summary: A model class of finite mixtures of linear additive models is presented. The component-specific parameters in the regression models are estimated using regularized likelihood methods. The advantages of the regularization are that (i) the pre-specified maximum degrees of freedom for the splines is less crucial than for unregularized estimation and that (ii) for each component individually a suitable degree of freedom is selected in an automatic way. The performance is evaluated in a simulation study with artificial data as well as on a yeast cell cycle dataset of gene expression levels over time. Availability: The latest release version of the R package flexmix is available from CRAN (http://cran.r-project.org/). Contact: Bettina.Gruen@jku.at Oxford University Press 2012-01-15 2011-11-26 /pmc/articles/PMC3259441/ /pubmed/22121159 http://dx.doi.org/10.1093/bioinformatics/btr653 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Grün, Bettina
Scharl, Theresa
Leisch, Friedrich
Modelling time course gene expression data with finite mixtures of linear additive models
title Modelling time course gene expression data with finite mixtures of linear additive models
title_full Modelling time course gene expression data with finite mixtures of linear additive models
title_fullStr Modelling time course gene expression data with finite mixtures of linear additive models
title_full_unstemmed Modelling time course gene expression data with finite mixtures of linear additive models
title_short Modelling time course gene expression data with finite mixtures of linear additive models
title_sort modelling time course gene expression data with finite mixtures of linear additive models
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3259441/
https://www.ncbi.nlm.nih.gov/pubmed/22121159
http://dx.doi.org/10.1093/bioinformatics/btr653
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