Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/106956
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dc.contributorDepartment of Electrical and Electronic Engineering-
dc.creatorWan, S-
dc.creatorMak, MW-
dc.date.accessioned2024-06-07T00:59:07Z-
dc.date.available2024-06-07T00:59:07Z-
dc.identifier.issn1868-8071-
dc.identifier.urihttp://hdl.handle.net/10397/106956-
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.rights© Springer-Verlag Berlin Heidelberg 2015en_US
dc.rightsThis version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use(https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms), but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: http://dx.doi.org/10.1007/s13042-015-0460-4.en_US
dc.subjectAdaptive decisionsen_US
dc.subjectMulti-label classificationen_US
dc.subjectProtein subcellular localizationen_US
dc.subjectSupport vector machinesen_US
dc.titlePredicting subcellular localization of multi-location proteins by improving support vector machines with an adaptive-decision schemeen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage399-
dc.identifier.epage411-
dc.identifier.volume9-
dc.identifier.issue3-
dc.identifier.doi10.1007/s13042-015-0460-4-
dcterms.abstractFrom the perspective of machine learning, predicting subcellular localization of multi-location proteins is a multi-label classification problem. Conventional multi-label classifiers typically compare some pattern-matching scores with a fixed decision threshold to determine the number of subcellular locations in which a protein will reside. This simple strategy, however, may easily lead to over-prediction due to a large number of false positives. To address this problem, this paper proposes a more powerful multi-label predictor, namely AD–SVM, which incorporates an adaptive-decision (AD) scheme into multi-label support vector machine (SVM) classifiers. Specifically, given a query protein, a term-frequency based gene ontology vector is constructed by successively searching the gene ontology annotation database. Subsequently, the feature vector is classified by AD–SVM, which extends the binary relevance method with an adaptive decision scheme that essentially converts the linear SVMs to piecewise linear SVMs. Experimental results suggest that AD–SVM outperforms existing state-of-the-art multi-location predictors by at least 4 % (absolute) for a stringent virus dataset and 1 % (absolute) for a stringent plant dataset, respectively. Results also show that the adaptive-decision scheme can effectively reduce over-prediction while having insignificant effect on the correctly predicted ones.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationInternational journal of machine learning and cybernetics, Mar. 2018, v. 9, no. 3, p. 399-411-
dcterms.isPartOfInternational journal of machine learning and cybernetics-
dcterms.issued2018-03-
dc.identifier.scopus2-s2.0-85008962067-
dc.identifier.eissn1868-808X-
dc.description.validate202405 bcch-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberEIE-0570en_US
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6713495en_US
dc.description.oaCategoryGreen (AAM)en_US
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