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dc.date.accessioned2021-04-22T20:16:26Z
dc.date.available2021-04-22T20:16:26Z
dc.date.created2020-10-15T19:49:30Z
dc.date.issued2020
dc.identifier.citationEngebretsen, Solveig Glad, Ingrid Kristine . Partially linear monotone methods with automatic variable selection and monotonicity direction discovery. Statistics in Medicine. 2020, 39(25), 3549-3568
dc.identifier.urihttp://hdl.handle.net/10852/85488
dc.description.abstractIn many statistical regression and prediction problems, it is reasonable to assume monotone relationships between certain predictor variables and the outcome. Genomic effects on phenotypes are, for instance, often assumed to be monotone. However, in some settings, it may be reasonable to assume a partially linear model, where some of the covariates can be assumed to have a linear effect. One example is a prediction model using both high‐dimensional gene expression data, and low‐dimensional clinical data, or when combining continuous and categorical covariates. We study methods for fitting the partially linear monotone model, where some covariates are assumed to have a linear effect on the response, and some are assumed to have a monotone (potentially nonlinear) effect. Most existing methods in the literature for fitting such models are subject to the limitation that they have to be provided the monotonicity directions a priori for the different monotone effects. We here present methods for fitting partially linear monotone models which perform both automatic variable selection, and monotonicity direction discovery. The proposed methods perform comparably to, or better than, existing methods, in terms of estimation, prediction, and variable selection performance, in simulation experiments in both classical and high‐dimensional data settings.
dc.languageEN
dc.titlePartially linear monotone methods with automatic variable selection and monotonicity direction discovery
dc.typeJournal article
dc.creator.authorEngebretsen, Solveig
dc.creator.authorGlad, Ingrid Kristine
cristin.unitcode185,15,13,0
cristin.unitnameMatematisk institutt
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode2
dc.identifier.cristin1839987
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Statistics in Medicine&rft.volume=39&rft.spage=3549&rft.date=2020
dc.identifier.jtitleStatistics in Medicine
dc.identifier.volume39
dc.identifier.issue25
dc.identifier.startpage3549
dc.identifier.endpage3568
dc.identifier.doihttps://doi.org/10.1002/sim.8680
dc.identifier.urnURN:NBN:no-88151
dc.type.documentTidsskriftartikkel
dc.source.issn0277-6715
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/85488/2/submitted_version_plamm.pdf
dc.type.versionSubmittedVersion
dc.relation.projectNFR/237718


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