Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/78294
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dc.titlePredicting coronary artery disease with medical profile and gene polymorphisms data
dc.contributor.authorChen, Q.
dc.contributor.authorLi, G.
dc.contributor.authorLeong, T.-Y.
dc.contributor.authorHeng, C.-K.
dc.date.accessioned2014-07-04T03:14:40Z
dc.date.available2014-07-04T03:14:40Z
dc.date.issued2007
dc.identifier.citationChen, Q.,Li, G.,Leong, T.-Y.,Heng, C.-K. (2007). Predicting coronary artery disease with medical profile and gene polymorphisms data. Studies in Health Technology and Informatics 129 : 1219-1224. ScholarBank@NUS Repository.
dc.identifier.isbn9781586037741
dc.identifier.issn09269630
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/78294
dc.description.abstractCoronary artery disease (CAD) is a main cause of death in the world. Finding cost-effective methods to predict CAD is a major challenge in public health. In this paper, we investigate the combined effects of genetic polymorphisms and non-genetic factors on predicting the risk of CAD by applying well known classification methods, such as Bayesian networks, naïve Bayes, support vector machine, k-nearest neighbor, neural networks and decision trees. Our experiments show that all these classifiers are comparable in terms of accuracy, while Bayesian networks have the additional advantage of being able to provide insights into the relationships among the variables. We observe that the learned Bayesian Networks identify many important dependency relationships among genetic variables, which can be verified with domain knowledge. Conforming to current domain understanding, our results indicate that related diseases (e.g., diabetes and hypertension), age and smoking status are the most important factors for CAD prediction, while the genetic polymorphisms entail more complicated influences. © 2007 The authors. All rights reserved.
dc.sourceScopus
dc.subjectBayesian networks
dc.subjectCoronary artery disease
dc.subjectdata mining
dc.subjectmachine learning
dc.subjectsingle nucleotide polymorphisms
dc.typeConference Paper
dc.contributor.departmentCOMPUTER SCIENCE
dc.contributor.departmentPAEDIATRICS
dc.description.sourcetitleStudies in Health Technology and Informatics
dc.description.volume129
dc.description.page1219-1224
dc.identifier.isiutNOT_IN_WOS
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