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dc.rights.licenseopenen_US
hal.structure.identifierStatistics In System biology and Translational Medicine [SISTM]
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorPRAGUE, Melanie
dc.contributor.authorLAVIELLE, Marc
dc.date.accessioned2022-06-15T14:32:47Z
dc.date.available2022-06-15T14:32:47Z
dc.date.issued2022-02
dc.identifier.issn2163-8306en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/140237
dc.description.abstractEnThe success of correctly identifying all the components of a nonlinear mixed-effects model is far from straightforward: it is a question of finding the best structural model, determining the type of relationship between covariates and individual parameters, detecting possible correlations between random effects, or also modeling residual errors. We present the SAMBA (Stochastic Approximation for Model Building Algorithm) procedure and show how this algorithm can be used to speed up this process of model building by identifying at each step how best to improve some of the model components. The principle of this algorithm basically consists in 'learning something' about the 'best model', even when a 'poor model' is used to fit the data. A comparison study of the SAMBA procedure with SCM and COSSAC show similar performances on several real data examples but with a much-reduced computing time. This algorithm is now implemented in Monolix and in the R package Rsmlx.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.enNonlinear models
dc.subject.enmixed-effects model
dc.subject.enPopulation PKPD
dc.subject.enModeling
dc.subject.enCovariate model selection
dc.subject.enStochastic algorithm
dc.title.enSAMBA: a Novel Method for Fast Automatic Model Building in Nonlinear Mixed-Effects Models
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/psp4.12742en_US
dc.subject.halMathématiques [math]/Systèmes dynamiques [math.DS]en_US
dc.subject.halMathématiques [math]/Statistiques [math.ST]en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.subject.halSciences du Vivant [q-bio]/Sciences pharmaceutiques/Pharmacologieen_US
dc.subject.halStatistiques [stat]/Méthodologie [stat.ME]en_US
dc.identifier.pubmed35104058en_US
bordeaux.journalCPT: Pharmacometrics and Systems Pharmacologyen_US
bordeaux.page161-172en_US
bordeaux.volume11en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamSISTM_BHPen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDMinistère de l'Enseignement supérieur, de la Recherche et de l'Innovationen_US
bordeaux.import.sourcehal
hal.identifierhal-03410025
hal.version1
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccCC BY-NCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=CPT:%20Pharmacometrics%20and%20Systems%20Pharmacology&rft.date=2022-02&rft.volume=11&rft.issue=2&rft.spage=161-172&rft.epage=161-172&rft.eissn=2163-8306&rft.issn=2163-8306&rft.au=PRAGUE,%20Melanie&LAVIELLE,%20Marc&rft.genre=article


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