Meta analysis of gene expression data of multiple cancer types to predict biomarkers and drug targets
Meta analysis of gene expression data of multiple cancer types such as breast, colon and ovary used to identify gene signatures that functionally used as a marker to prognosis and molecular diagnostics. There is a reliable identification of gene signatures is associated with different cancer types r...
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Published in | Computational molecular biology Vol. 5; no. 5 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Richmond
Sophia Publishing Group Inc
01.01.2015
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Online Access | Get full text |
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Summary: | Meta analysis of gene expression data of multiple cancer types such as breast, colon and ovary used to identify gene signatures that functionally used as a marker to prognosis and molecular diagnostics. There is a reliable identification of gene signatures is associated with different cancer types remains a challenge. The aim of this study is to develop microarray statistical data analysis methods and SVM classifiers to identify differentially expressed genes in different cancer types. Using our method to perform 16 datasets such as 6 breast cancer, 4 colon cancer and 6 ovarian cancer of different datasets. Our results is analysed in 4 different methods (a) preprocess the data to identify quality expression of datasets by removing null values and non significant values (p<0.05) (b). Differential gene expression analysis using statistical analysis to predict upregulation and downregulated gene signatures (c) subgrouping of datasets that has been classified based on cancer types (d) gene network prediction to identify gene-gene interaction to understand biological markers. We have predicted 8 markers in breast cancer, 10 markers in colon cancer and 16 markers in ovarian cancer is providing new direction for diagnostics and therapeutic development. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1927-5587 1927-5587 |
DOI: | 10.5376/cmb.2015.05.0005 |