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dc.contributor.authorRaza, Ali
dc.contributor.authorRustam, Furqan
dc.contributor.authorSiddiqui, Hafeez Ur Rehman
dc.contributor.authorTorre Díez, Isabel de la 
dc.contributor.authorGarcia Zapirain, Begonya
dc.contributor.authorLee, Ernesto
dc.contributor.authorAshraf, Imran
dc.date.accessioned2023-08-16T08:23:34Z
dc.date.available2023-08-16T08:23:34Z
dc.date.issued2023
dc.identifier.citationGenes, 2023, Vol. 14, Nº. 1, 71es
dc.identifier.issn2073-4425es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/60685
dc.descriptionProducción Científicaes
dc.description.abstractGenetic disorders are the result of mutation in the deoxyribonucleic acid (DNA) sequence which can be developed or inherited from parents. Such mutations may lead to fatal diseases such as Alzheimer’s, cancer, Hemochromatosis, etc. Recently, the use of artificial intelligence-based methods has shown superb success in the prediction and prognosis of different diseases. The potential of such methods can be utilized to predict genetic disorders at an early stage using the genome data for timely treatment. This study focuses on the multi-label multi-class problem and makes two major contributions to genetic disorder prediction. A novel feature engineering approach is proposed where the class probabilities from an extra tree (ET) and random forest (RF) are joined to make a feature set for model training. Secondly, the study utilizes the classifier chain approach where multiple classifiers are joined in a chain and the predictions from all the preceding classifiers are used by the conceding classifiers to make the final prediction. Because of the multi-label multi-class data, macro accuracy, Hamming loss, and α-evaluation score are used to evaluate the performance. Results suggest that extreme gradient boosting (XGB) produces the best scores with a 92% α-evaluation score and a 84% macro accuracy score. The performance of XGB is much better than state-of-the-art approaches, in terms of both performance and computational complexity.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherMDPIes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectGeneticses
dc.subjectHuman geneticses
dc.subjectGenética humanaes
dc.subjectMutation (Biologie)es
dc.subjectMutación (Biología)es
dc.subjectGenetic disorderses
dc.subjectMachine learninges
dc.subjectAprendizaje automáticoes
dc.subject.classificationChain classifier approaches
dc.subject.classificationEnfoque clasificador de cadenaes
dc.titlePredicting genetic disorder and types of disorder using chain classifier approaches
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2022 The Authorses
dc.identifier.doi10.3390/genes14010071es
dc.relation.publisherversionhttps://www.mdpi.com/2073-4425/14/1/71es
dc.identifier.publicationfirstpage71es
dc.identifier.publicationissue1es
dc.identifier.publicationtitleGeneses
dc.identifier.publicationvolume14es
dc.peerreviewedSIes
dc.identifier.essn2073-4425es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones
dc.subject.unesco2409 Genéticaes
dc.subject.unesco2409.02 Ingeniería Genéticaes


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