Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0097079
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dc.titleEnsemble positive unlabeled learning for disease gene identification
dc.contributor.authorYang P.
dc.contributor.authorLi X.
dc.contributor.authorChua H.-N.
dc.contributor.authorKwoh C.-K.
dc.contributor.authorNg S.-K.
dc.date.accessioned2019-11-05T00:37:28Z
dc.date.available2019-11-05T00:37:28Z
dc.date.issued2014
dc.identifier.citationYang P., Li X., Chua H.-N., Kwoh C.-K., Ng S.-K. (2014). Ensemble positive unlabeled learning for disease gene identification. PLoS ONE 9 (5) : e97079. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0097079
dc.identifier.issn1932-6203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161412
dc.description.abstractAn increasing number of genes have been experimentally confirmed in recent years as causative genes to various human diseases. The newly available knowledge can be exploited by machine learning methods to discover additional unknown genes that are likely to be associated with diseases. In particular, positive unlabeled learning (PU learning) methods, which require only a positive training set P (confirmed disease genes) and an unlabeled set U (the unknown candidate genes) instead of a negative training set N, have been shown to be effective in uncovering new disease genes in the current scenario. Using only a single source of data for prediction can be susceptible to bias due to incompleteness and noise in the genomic data and a single machine learning predictor prone to bias caused by inherent limitations of individual methods. In this paper, we propose an effective PU learning framework that integrates multiple biological data sources and an ensemble of powerful machine learning classifiers for disease gene identification. Our proposed method integrates data from multiple biological sources for training PU learning classifiers. A novel ensemble-based PU learning method EPU is then used to integrate multiple PU learning classifiers to achieve accurate and robust disease gene predictions. Our evaluation experiments across six disease groups showed that EPU achieved significantly better results compared with various state-of-the-art prediction methods as well as ensemble learning classifiers. Through integrating multiple biological data sources for training and the outputs of an ensemble of PU learning classifiers for prediction, we are able to minimize the potential bias and errors in individual data sources and machine learning algorithms to achieve more accurate and robust disease gene predictions. In the future, our EPU method provides an effective framework to integrate the additional biological and computational resources for better disease gene predictions. © 2014 Yang et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectarticle
dc.subjectcardiovascular disease
dc.subjectclassification algorithm
dc.subjectcomparative study
dc.subjectendocrine disease
dc.subjectensemble positive unlabeled learning
dc.subjecteye disease
dc.subjectgene expression
dc.subjectgene identification
dc.subjectgene ontology
dc.subjectgenetic similarity
dc.subjectgenotype phenotype correlation
dc.subjectlearning algorithm
dc.subjectmachine learning
dc.subjectmeasurement accuracy
dc.subjectmetabolic disorder
dc.subjectneoplasm
dc.subjectneurologic disease
dc.subjectprediction
dc.subjectprotein interaction
dc.subjectsensitivity analysis
dc.subjectalgorithm
dc.subjectartificial intelligence
dc.subjectbiological model
dc.subjectbiology
dc.subjectevaluation study
dc.subjectgene regulatory network
dc.subjectgenetic association
dc.subjectgenetic disorder
dc.subjectgenetics
dc.subjecthuman
dc.subjectphenotype
dc.subjectprocedures
dc.subjectselection bias
dc.subjecttrends
dc.subjectAlgorithms
dc.subjectArtificial Intelligence
dc.subjectComputational Biology
dc.subjectGene Ontology
dc.subjectGene Regulatory Networks
dc.subjectGenetic Association Studies
dc.subjectGenetic Diseases, Inborn
dc.subjectHumans
dc.subjectModels, Genetic
dc.subjectPhenotype
dc.subjectSelection Bias
dc.typeArticle
dc.contributor.departmentDEPARTMENT OF COMPUTER SCIENCE
dc.description.doi10.1371/journal.pone.0097079
dc.description.sourcetitlePLoS ONE
dc.description.volume9
dc.description.issue5
dc.description.pagee97079
dc.published.statePublished
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