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A candidate-set-free algorithm for generating D-optimal split-plot designs

We introduce a new method for generating optimal split-plot designs. These designs are optimal in the sense that they are efficient for estimating the fixed effects of the statistical model that is appropriate given the split-plot design structure. One advantage of the method is that it does not req...

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Detalles Bibliográficos
Autores principales: Jones, Bradley, Goos, Peter
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001117/
https://www.ncbi.nlm.nih.gov/pubmed/21197132
http://dx.doi.org/10.1111/j.1467-9876.2007.00581.x
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author Jones, Bradley
Goos, Peter
author_facet Jones, Bradley
Goos, Peter
author_sort Jones, Bradley
collection PubMed
description We introduce a new method for generating optimal split-plot designs. These designs are optimal in the sense that they are efficient for estimating the fixed effects of the statistical model that is appropriate given the split-plot design structure. One advantage of the method is that it does not require the prior specification of a candidate set. This makes the production of split-plot designs computationally feasible in situations where the candidate set is too large to be tractable. The method allows for flexible choice of the sample size and supports inclusion of both continuous and categorical factors. The model can be any linear regression model and may include arbitrary polynomial terms in the continuous factors and interaction terms of any order. We demonstrate the usefulness of this flexibility with a 100-run polypropylene experiment involving 11 factors where we found a design that is substantially more efficient than designs that are produced by using other approaches.
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spelling pubmed-30011172010-12-31 A candidate-set-free algorithm for generating D-optimal split-plot designs Jones, Bradley Goos, Peter J R Stat Soc Ser C Appl Stat Original Articles We introduce a new method for generating optimal split-plot designs. These designs are optimal in the sense that they are efficient for estimating the fixed effects of the statistical model that is appropriate given the split-plot design structure. One advantage of the method is that it does not require the prior specification of a candidate set. This makes the production of split-plot designs computationally feasible in situations where the candidate set is too large to be tractable. The method allows for flexible choice of the sample size and supports inclusion of both continuous and categorical factors. The model can be any linear regression model and may include arbitrary polynomial terms in the continuous factors and interaction terms of any order. We demonstrate the usefulness of this flexibility with a 100-run polypropylene experiment involving 11 factors where we found a design that is substantially more efficient than designs that are produced by using other approaches. Blackwell Publishing Ltd 2007-05 /pmc/articles/PMC3001117/ /pubmed/21197132 http://dx.doi.org/10.1111/j.1467-9876.2007.00581.x Text en © 2007 Royal Statistical Society http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Jones, Bradley
Goos, Peter
A candidate-set-free algorithm for generating D-optimal split-plot designs
title A candidate-set-free algorithm for generating D-optimal split-plot designs
title_full A candidate-set-free algorithm for generating D-optimal split-plot designs
title_fullStr A candidate-set-free algorithm for generating D-optimal split-plot designs
title_full_unstemmed A candidate-set-free algorithm for generating D-optimal split-plot designs
title_short A candidate-set-free algorithm for generating D-optimal split-plot designs
title_sort candidate-set-free algorithm for generating d-optimal split-plot designs
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001117/
https://www.ncbi.nlm.nih.gov/pubmed/21197132
http://dx.doi.org/10.1111/j.1467-9876.2007.00581.x
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