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Article: Novel hybrid method for gene selection and cancer prediction

TitleNovel hybrid method for gene selection and cancer prediction
Authors
KeywordsClassification
Cancer Prediction
Gene Selection
Lasso
Clustering
Issue Date2010
Citation
World Academy of Science, Engineering and Technology, 2010, v. 62, p. 482-489 How to Cite?
AbstractMicroarray data profiles gene expression on a whole genome scale, therefore, it provides a good way to study associations between gene expression and occurrence or progression of cancer. More and more researchers realized that microarray data is helpful to predict cancer sample. However, the high dimension of gene expressions is much larger than the sample size, which makes this task very difficult. Therefore, how to identify the significant genes causing cancer becomes emergency and also a hot and hard research topic. Many feature selection algorithms have been proposed in the past focusing on improving cancer predictive accuracy at the expense of ignoring the correlations between the features. In this work, a novel framework (named by SGS) is presented for stable gene selection and efficient cancer prediction. The proposed framework first performs clustering algorithm to find the gene groups where genes in each group have higher correlation coefficient, and then selects the significant genes in each group with Bayesian Lasso and important gene groups with group Lasso, and finally builds prediction model based on the shrinkage gene space with efficient classification algorithm (such as, SVM, 1NN, Regression and etc.). Experiment results on real world data show that the proposed framework often outperforms the existing feature selection and prediction methods, say SAM, IG and Lasso-type prediction model.
Persistent Identifierhttp://hdl.handle.net/10722/276886
ISSN

 

DC FieldValueLanguage
dc.contributor.authorJing, Liping-
dc.contributor.authorNg, Michael K.-
dc.contributor.authorZeng, Tieyong-
dc.date.accessioned2019-09-18T08:34:57Z-
dc.date.available2019-09-18T08:34:57Z-
dc.date.issued2010-
dc.identifier.citationWorld Academy of Science, Engineering and Technology, 2010, v. 62, p. 482-489-
dc.identifier.issn2010-376X-
dc.identifier.urihttp://hdl.handle.net/10722/276886-
dc.description.abstractMicroarray data profiles gene expression on a whole genome scale, therefore, it provides a good way to study associations between gene expression and occurrence or progression of cancer. More and more researchers realized that microarray data is helpful to predict cancer sample. However, the high dimension of gene expressions is much larger than the sample size, which makes this task very difficult. Therefore, how to identify the significant genes causing cancer becomes emergency and also a hot and hard research topic. Many feature selection algorithms have been proposed in the past focusing on improving cancer predictive accuracy at the expense of ignoring the correlations between the features. In this work, a novel framework (named by SGS) is presented for stable gene selection and efficient cancer prediction. The proposed framework first performs clustering algorithm to find the gene groups where genes in each group have higher correlation coefficient, and then selects the significant genes in each group with Bayesian Lasso and important gene groups with group Lasso, and finally builds prediction model based on the shrinkage gene space with efficient classification algorithm (such as, SVM, 1NN, Regression and etc.). Experiment results on real world data show that the proposed framework often outperforms the existing feature selection and prediction methods, say SAM, IG and Lasso-type prediction model.-
dc.languageeng-
dc.relation.ispartofWorld Academy of Science, Engineering and Technology-
dc.subjectClassification-
dc.subjectCancer Prediction-
dc.subjectGene Selection-
dc.subjectLasso-
dc.subjectClustering-
dc.titleNovel hybrid method for gene selection and cancer prediction-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.scopuseid_2-s2.0-78651594051-
dc.identifier.volume62-
dc.identifier.spage482-
dc.identifier.epage489-
dc.identifier.eissn2010-3778-

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