Please use this identifier to cite or link to this item: http://hdl.handle.net/10662/20418
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dc.contributor.authorDíaz Álvarez, Josefa-
dc.contributor.authorMatias-Guiu Antem, Jordi A.-
dc.contributor.authorCabrera Martín, María Nieves-
dc.contributor.authorRisco Martín, José Luis-
dc.contributor.authorAyala Rodríguez, José Luis-
dc.date.accessioned2024-02-08T10:17:43Z-
dc.date.available2024-02-08T10:17:43Z-
dc.date.issued2019-10-11-
dc.identifier.issn1471-2105-
dc.identifier.urihttp://hdl.handle.net/10662/20418-
dc.description.abstractThis reseach work focuses on the analysis of health and medical data is crucial for improving the diagnosis precision, treatments and prevention. In this field, machine learning techniques play a key role. However, the amount of health data acquired from digital machines has high dimensionality and not all data acquired from digital machines are relevant for a particular disease. Primary Progressive Aphasia (PPA) is a neurodegenerative syndrome including several specific diseases, and it is a good model to implement machine learning analyses. In this work, we applied five feature selection algorithms to identify the set of relevant features from 18F-fluorodeoxyglucose positron emission tomography images of the main areas affected by PPA from patient records. On the other hand, we carried out classification and clustering algorithms before and after the feature selection process to contrast both results with those obtained in a previous work. We aimed to find the best classifier and the more relevant features from the WEKA tool to propose further a framework for automatic help on diagnosis. Dataset contains data from 150 FDG-PET imaging studies of 91 patients with a clinic prognosis of PPA, which were examined twice, and 28 controls. Our method comprises six different stages: (i) feature extraction, (ii) expertise knowledge supervision (iii) classification process, (iv) comparing classification results for feature selection, (v) clustering process after feature selection, and (vi) comparing clustering results with those obtained in a previous work. Experimental tests confirmed clustering results from a previous work. Although classification results for some algorithms are not decisive for reducing features precisely, Principal Components Analisys (PCA) results exhibited similar or even better performances when compared to those obtained with all features. As a conclusion, although reducing the dimensionality does not mean a general improvement, the set of features is almost halved and results are better or quite similar. Finally, it is interesting how these results expose a finer grain classification of patients according to the neuroanatomy of their disease.es_ES
dc.description.sponsorshipWe acknowledge support from Spanish Ministry of Economy and Competitiveness and European Regional Development Fund (FEDER) under project TIN2017-85727-C4-4-P, and by the project IB16035 of the Regional Government of Extremadura, Department of Commerce and Economy, co-financed by the European Regional Development Fund, "A way to build Europe".. . .es_ES
dc.format.extent12es_ES
dc.format.mimetypeapplication/pdfen_US
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMachine learninges_ES
dc.subjectprimary progressive aphasiaes_ES
dc.subjectSupervised algorithmes_ES
dc.subjectUnsupervised algorithmes_ES
dc.subjectClustering Analysises_ES
dc.titleAn application of machine learning with feature selection to improve diagnosis and classification of neurodegenerative disorderses_ES
dc.typearticlees_ES
dc.description.versionpeerReviewedes_ES
europeana.typeTEXTen_US
dc.rights.accessRightsopenAccesses_ES
dc.subject.unesco3304 Tecnología de Los Ordenadoreses_ES
dc.subject.unesco32 Ciencias Médicases_ES
europeana.dataProviderUniversidad de Extremadura. Españaes_ES
dc.type.versionpublishedVersiones_ES
dc.contributor.affiliationUniversidad de Extremadura. Departamento de Tecnología de los Computadores y de las Comunicacioneses_ES
dc.relation.publisherversionhttps://doi.org/10.1186/s12859-019-3027-7es_ES
dc.identifier.publicationtitleBMC Bioinformaticses_ES
dc.identifier.publicationfirstpage491es_ES
dc.identifier.publicationlastpage503es_ES
dc.identifier.publicationvolume20es_ES
dc.identifier.orcid0000-0003-2105-3905es_ES
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