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dc.contributor.authorLiu, Qingzhong
dc.contributor.authorSung, Andrew H.
dc.contributor.authorChen, Zhongxue
dc.contributor.authorLiu, Jianzhong
dc.contributor.authorDeng, Youping
dc.contributor.authorHuang, Xudong
dc.date.accessioned2011-11-22T16:23:01Z
dc.date.issued2009
dc.identifier.citationLiu, Qingzhong, Andrew H. Sung, Zhongxue Chen, Jianzhong Liu, Xudong Huang, and Youping Deng. 2009. Feature Selection and Classification of MAQC-II Breast Cancer and Multiple Myeloma Microarray Gene Expression Data. PLoS ONE 4(12): e8250.en_US
dc.identifier.issn1932-6203en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:5350702
dc.description.abstractMicroarray data has a high dimension of variables but available datasets usually have only a small number of samples, thereby making the study of such datasets interesting and challenging. In the task of analyzing microarray data for the purpose of, e.g., predicting gene-disease association, feature selection is very important because it provides a way to handle the high dimensionality by exploiting information redundancy induced by associations among genetic markers. Judicious feature selection in microarray data analysis can result in significant reduction of cost while maintaining or improving the classification or prediction accuracy of learning machines that are employed to sort out the datasets. In this paper, we propose a gene selection method called Recursive Feature Addition (RFA), which combines supervised learning and statistical similarity measures. We compare our method with the following gene selection methods: Support Vector Machine Recursive Feature Elimination (SVMRFE) Leave-One-Out Calculation Sequential Forward Selection (LOOCSFS) Gradient based Leave-one-out Gene Selection (GLGS) To evaluate the performance of these gene selection methods, we employ several popular learning classifiers on the MicroArray Quality Control phase II on predictive modeling (MAQC-II) breast cancer dataset and the MAQC-II multiple myeloma dataset. Experimental results show that gene selection is strictly paired with learning classifier. Overall, our approach outperforms other compared methods. The biological functional analysis based on the MAQC-II breast cancer dataset convinced us to apply our method for phenotype prediction. Additionally, learning classifiers also play important roles in the classification of microarray data and our experimental results indicate that the Nearest Mean Scale Classifier (NMSC) is a good choice due to its prediction reliability and its stability across the three performance measurements: Testing accuracy, MCC values, and AUC errors.en_US
dc.language.isoen_USen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofdoi:10.1371/journal.pone.0008250en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789385/pdf/en_US
dash.licenseLAA
dc.subjectcomputational biologyen_US
dc.subjectgenomicsen_US
dc.subjectmetagenomicsen_US
dc.subjectsystems biologyen_US
dc.subjectcomputer scienceen_US
dc.subjectapplicationsen_US
dc.titleFeature Selection and Classification of MAQC-II Breast Cancer and Multiple Myeloma Microarray Gene Expression Dataen_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalPLoS ONEen_US
dash.depositing.authorHuang, Xudong
dc.date.available2011-11-22T16:23:01Z
dash.affiliation.otherHMS^Radiology-Brigham and Women's Hospitalen_US
dc.identifier.doi10.1371/journal.pone.0008250*
dash.authorsorderedfalse
dash.contributor.affiliatedHuang, Xudong


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