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Prediction model building and feature selection with SVM in breast cancer diagnosis Cheng-Lung Huang, Hung-Chang Liao, Mu- Chen Chen Expert Systems with Applications 2008
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Introduction Breast cancer is a serious problem for the young women of Taiwan. Almost 64.1% of women with breast cancer are diagnosed before the age of 50 and 29.3% of women with breast cancer are diagnosed before the age of 40. However, the causes are still unknown.
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Introduction This study (Ziegler et al., 1993) shows that fibroadenoma shared some risk factors with breast cancer. HSV-1 (herpes simplex virus type 1) EBV (Epstein-Barr virus) CMV (cytomegalovirus) HPV (human papillomavirus) HHV-8 (human herpesvirus-8)
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Introduction DNA viruses, as causes, are closely related to the human cancers as part of the high-risk factors. In order to obtain the relationship between DNA viruses and breast tumors. This paper uses the support vector machines (SVM) to find the pertinent bioinformatics.
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Two Important Challenge When using SVM, two problems are confronted: How to choose the optimal input feature subset for SVM. How to set the best kernel parameters. These two problems are crucial because the feature subset choice influences the appropriate kernel parameters and vice versa.
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Feature Selection Feature selection is an important issue in building classification systems. It is advantageous to limit the number of input features in a classifier in order to have a good predictive and less computationally intensive model. This study tried F-score calculation to select input features.
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F-Score
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F-Score Algorithm
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Parameters Optimization To design a SVM, one must choose a kernel function,set the kernel parameters and determine a soft margin constant C. The grid algorithm is an alternative to finding the best C and gamma when using the RBF kernel function. This study tried grid search to find the best SVM model parameters.
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Grid-Search Algorithm
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Data collection The source of 80 data points (tissue samples) 52 specimens of non-familial invasive ductal breast cancer. 28 mammary fibroadenomas. (From Chung-Shan Medical University Hospital )
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Data partition Data set is further randomly partitioned into training and independent testing sets via a stratified 5-fold cross validation.
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SVM-based optimize parameters and feature selection
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The relative feature importance with F-score
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The relative importance of DNA virus based on the F-score
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The five feature subsets based on the F-score
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Overall training and testing accuracy for each feature subset
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Type I and type II errors Type I errors (the "false positive"): the error of rejecting the null hypothesis given that it is actually true Type II errors (the "false negative"): the error of failing to reject the null hypothesis given that the alternative hypothesis is actually true
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Detail testing accuracy for feature subset of size 2 and 3
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Linear discriminate analysis (LDA) Originally developed in 1936 by R.A. Fisher, Discriminate Analysis is a classic method of classification. Discriminate analysis can be used only for classification Linear discriminant analysis finds a linear transformation ("discriminant function") of the two predictors, X and Y, that yields a new set of transformed values that provides a more accurate discrimination than either predictor alone: Transformed Target = C1*X + C2*Y
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The P-level of each attribute for LDA Selection criteria: P-level value < 0.05
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Training and testing accuracy for LDA
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Comparison summary between SVM and LDA
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Conclusion In order to find the correlation DNA viruses with breast tumor, and to achieve a high classificatory accuracy. F-score is adapted to find the important features. grid search approach is used to search the optimal SVM parameters. The results revealed that the SVM-based model has good performance in diagnosing breast cancer according to our data set.
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Conclusion The present study’s results also show that the attributes{HSV-1, HHV-8} or {HSV-1, HHV-8, CMV} can achieve identical high accuracy, at 86% of average overall hit rate. This study suggests simultaneously considering HSV-1 and HHV-8 is feasible; however, only considering HHV-8 or HSV-1 is less accurate.
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Future Work The practical obstacle of the SVM-based (as well as neural networks) classification model is its black-box nature. A possible solution for this issue is the use of SVM rule extraction techniques or the use of hybrid-SVM model combined with other more interpretable models.
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Thank You
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