A breast cancer diagnosis system: a combined approach using rough sets and probabilistic neural networks

In this paper, we present a medical decision support system based on a hybrid approach utilising rough sets and a probabilistic neural network. We utilised the ability of rough sets to perform dimensionality reduction to eliminate redundant attributes from a biomedical dataset. We then utilised a probabilistic neural network to perform supervised classification. Our results indicate that rough sets was able to reduce the number of attributes in the dataset by 67% without sacrificing classification accuracy. Our classification accuracy results yielded results on the order of 93%

Staging of Prostate Cancer Using Automatic Feature Selection, Sampling and Dempster-Shafer Fusion

A novel technique of automatically selecting the best pairs of features and sampling techniques to predict the stage of prostate cancer is proposed in this study. The problem of class imbalance, which is prominent in most medical data sets is also addressed here. Three feature subsets obtained by the use of principal components analysis (PCA), genetic algorithm (GA) and rough sets (RS) based approaches were also used in the study. The performance of under-sampling, synthetic minority over-sampling technique (SMOTE) and a combination of the two were also investigated and the performance of the obtained models was compared. To combine the classifier outputs, we used the Dempster-Shafer (DS) theory, whereas the actual choice of combined models was made using a GA. We found that the best performance for the overall system resulted from the use of under sampled data combined with rough sets based features modeled as a support vector machine (SVM)

Microarray-Based Cancer Prediction Using Soft Computing Approach

One of the difficulties in using gene expression profiles to predict cancer is how to effectively select a few informative genes to construct accurate prediction models from thousands or ten thousands of genes. We screen highly discriminative genes and gene pairs to create simple prediction models involved in single genes or gene pairs on the basis of soft computing approach and rough set theory. Accurate cancerous prediction is obtained when we apply the simple prediction models for four cancerous gene expression datasets: CNS tumor, colon tumor, lung cancer and DLBCL. Some genes closely correlated with the pathogenesis of specific or general cancers are identified. In contrast with other models, our models are simple, effective and robust. Meanwhile, our models are interpretable for they are based on decision rules. Our results demonstrate that very simple models may perform well on cancerous molecular prediction and important gene markers of cancer can be detected if the gene selection approach is chosen reasonably