Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2164-9-S2-S18
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dc.titleA stable iterative method for refining discriminative gene clusters
dc.contributor.authorXu, M.
dc.contributor.authorZhu, M.
dc.contributor.authorZhang, L.
dc.date.accessioned2014-10-28T02:50:24Z
dc.date.available2014-10-28T02:50:24Z
dc.date.issued2008-09-16
dc.identifier.citationXu, M., Zhu, M., Zhang, L. (2008-09-16). A stable iterative method for refining discriminative gene clusters. BMC Genomics 9 (SUPPL. 2) : -. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2164-9-S2-S18
dc.identifier.issn14712164
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/104523
dc.description.abstractBackground: Microarray technology is often used to identify the genes that are differentially expressed between two biological conditions. On the other hand, since microarray datasets contain a small number of samples and a large number of genes, it is usually desirable to identify small gene subsets with distinct pattern between sample classes. Such gene subsets are highly discriminative in phenotype classification because of their tightly coupling features. Unfortunately, such identified classifiers usually tend to have poor generalization properties on the test samples due to overfitting problem. Results: We propose a novel approach combining both supervised learning with unsupervised learning techniques to generate increasingly discriminative gene clusters in an iterative manner. Our experiments on both simulated and real datasets show that our method can produce a series of robust gene clusters with good classification performance compared with existing approaches. Conclusion: This backward approach for refining a series of highly discriminative gene clusters for classification purpose proves to be very consistent and stable when applied to various types of training samples. © 2008 Xu et al; licensee BioMed Central Ltd.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1186/1471-2164-9-S2-S18
dc.sourceScopus
dc.typeConference Paper
dc.contributor.departmentMATHEMATICS
dc.description.doi10.1186/1471-2164-9-S2-S18
dc.description.sourcetitleBMC Genomics
dc.description.volume9
dc.description.issueSUPPL. 2
dc.description.page-
dc.description.codenBGMEE
dc.identifier.isiut000206244200019
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