Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/1721.1/7238
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dc.creatorYeo, Gene-
dc.creatorPoggio, Tomaso-
dc.date2004-10-20T21:03:45Z-
dc.date2004-10-20T21:03:45Z-
dc.date2001-08-25-
dc.date.accessioned2013-10-09T02:48:37Z-
dc.date.available2013-10-09T02:48:37Z-
dc.date.issued2013-10-09-
dc.identifierAIM-2001-018-
dc.identifierCBCL-206-
dc.identifierhttp://hdl.handle.net/1721.1/7238-
dc.identifier.urihttp://koha.mediu.edu.my:8181/xmlui/handle/1721-
dc.descriptionA novel approach to multiclass tumor classification using Artificial Neural Networks (ANNs) was introduced in a recent paper cite{Khan2001}. The method successfully classified and diagnosed small, round blue cell tumors (SRBCTs) of childhood into four distinct categories, neuroblastoma (NB), rhabdomyosarcoma (RMS), non-Hodgkin lymphoma (NHL) and the Ewing family of tumors (EWS), using cDNA gene expression profiles of samples that included both tumor biopsy material and cell lines. We report that using an approach similar to the one reported by Yeang et al cite{Yeang2001}, i.e. multiclass classification by combining outputs of binary classifiers, we achieved equal accuracy with much fewer features. We report the performances of 3 binary classifiers (k-nearest neighbors (kNN), weighted-voting (WV), and support vector machines (SVM)) with 3 feature selection techniques (Golub's Signal to Noise (SN) ratios cite{Golub99}, Fisher scores (FSc) and Mukherjee's SVM feature selection (SVMFS))cite{Sayan98}.-
dc.format17 p.-
dc.format6552074 bytes-
dc.format816114 bytes-
dc.formatapplication/postscript-
dc.formatapplication/pdf-
dc.languageen_US-
dc.relationAIM-2001-018-
dc.relationCBCL-206-
dc.subjectAI-
dc.subjectmulticlass-
dc.subjectSVM-
dc.subjectfeature selection-
dc.subjectSRBCT-
dc.subjecttumors-
dc.titleMulticlass Classification of SRBCTs-
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