This paper proposes a weighted Support Vector Machine (w-SVM) method for efficient class prediction in binary response data sets. The proposed method was obtained by introducing weights which utilizes the point biserial correlation between each of the predictors and the dichotomized response variable into the standard SVM algorithm to maximize the classification accuracy. The optimal value of the proposed w-SVM cost and each of the kernels parameters were determined by grid search in a 10-fold cross validation resampling method. Monte-Carlo Cross Validation method was employed to examine the predictive power of the proposed method by partitioning the data into train and test samples using different sampling splitting ratios. Application of the proposed method on the simulated data sets yielded high prediction accuracy on the test sample. Results from other performance indices further gave credence to the efficiency of the proposed method. The performance of the proposed method was compared with three of the state-of-the art machine learning methods including the standard SVM and the result showed the superiority of this method over others. Finally, the results generally show that the modified algorithm with Radial Basis Function (RBF) Kernel perform excellently and achieved the best predictive performance than any of the existing classifiers considered.
Background: The computerised classification and prediction of heart disease can be useful for medical personnel for the purpose of fast diagnosis with accurate results. This study presents an efficient classification method for predicting heart disease using a data-mining algorithm. Methods: The algorithm utilises the weighted support vector machine method for efficient classification of heart disease based on a binary response that indicates the presence or absence of heart disease as the result of an angiographic test. The optimal values of the support vector machine and the Radial Basis Function kernel parameters for the heart disease classification were determined via a 10-fold cross-validation method. The heart disease data was partitioned into training and testing sets using different percentages of the splitting ratio. Each of the training sets was used in training the classification method while the predictive power of the method was evaluated on each of the test sets using the Monte-Carlo cross-validation resampling technique. The effect of different percentages of the splitting ratio on the method was also observed. Results: The misclassification error rate was used to compare the performance of the method with three selected machine learning methods and was observed that the proposed method performs best over others in all cases considered. Conclusion: Finally, the results illustrate that the classification algorithm presented can effectively predict the heart disease status of an individual based on the results of an angiographic test.
Background & Aim: In this study, efficient Support Vector Machine (SVM) algorithm for feature selection and classification of multi-category tumour classes of biological samples using gene expression profiles was proposed. Methods: Feature selection interface of the algorithm employed the F-statistic of the ANOVA–like testing scheme at some chosen family-wise-error-rate which ensured efficient detection of false-positive genes. The selected gene subsets using the above method were further screened for optimality using the Misclassification Error Rates yielded by each of them and their combinations in a sequential selection manner. In a 10-fold cross-validation, the optimal values of the SVM parameters with appropriate kernel were determined for tissue sample classification using one-versus-all approach. The entire data matrix was randomly partitioned into 95% training set to train the SVM classifier and 5% test set to evaluate the predictive performance of the classifier over 1,000 Monte-Carlo cross-validation runs. Published microarray breast cancer dataset with five clinical endpoints was employed to validate the results from the simulation studies. Results: Results from Monte-Carlo study showed excellent performance of the SVM classifier with higher prediction accuracy of the tissue samples based on the few gene biomarkers selected by the proposed feature selection method. Conclusion: SVM could be considered as a classification of multi-category tumour classes of biological
Objective: This paper aims to present a novel procedure for testing a set of population proportions against an ordered alternative with a control. Material and Methods: The distribution of the test statistic for the proposed test was determined theoretically and through Monte-Carlo experiments. The efficiency of the proposed test method was compared with the classical Chi-square test of homogeneity of population proportions using their empirical Type I error rates and powers at various sample sizes. Results: The new test statistic that was developed for testing a set of population proportions against an ordered alternative with a control was found to have a Chi-square distribution with non-integer values degrees of freedom v that depend on the number of population groups k being compared. Table of values of v for comparing up to 26 population groups was constructed while an expression was developed to determine v for cases where k > 26. Further results showed that the new test method is capable of detecting the superiority of a treatment, for instance a new drug type, over some of the existing ones in situations where only the qualitative data on users' preferences of all the available treatments (drug types) are available. The new test method was found to be relatively more powerful and consistent at estimating the nominal Type I error rates (α), especially at smaller sample sizes than the classical Chi-square test of homogeneity of population proportions. Conclusion: The new test method proposed here could find applications in pharmacology where a newly developed drug might be expected to be more preferred by users than some of the existing ones. This kind of test problem can equally exist in medicine, engineering and humanities in situations where only the qualitative data on users' preferences of a set of treatments or systems are available.
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