Abstract

Early detection of cancer increases the probability of recovery. This paper presents an intelligent decision support system (IDSS) for the early diagnosis of cancer based on gene expression profiles collected using DNA microarrays. Such datasets pose a challenge because of the small number of samples (no more than a few hundred) relative to the large number of genes (in the order of thousands). Therefore, a method of reducing the number of features (genes) that are not relevant to the disease of interest is necessary to avoid overfitting. The proposed methodology uses the information gain (IG) to select the most important features from the input patterns. Then, the selected features (genes) are reduced by applying the grey wolf optimization (GWO) algorithm. Finally, the methodology employs a support vector machine (SVM) classifier for cancer type classification. The proposed methodology was applied to two datasets (Breast and Colon) and was evaluated based on its classification accuracy, which is the most important performance measure in disease diagnosis. The experimental results indicate that the proposed methodology is able to enhance the stability of the classification accuracy as well as the feature selection.

Highlights

  • Cancer is a common disease caused by certain abnormal changes to genes that are responsible for cell division and growth

  • This paper addresses the problem of medical diagnosis and presents an intelligent decision support system (IDSS) for cancer diagnosis based on gene expression profiles from DNA microarray datasets

  • This paper proposes an IDSS for central nervous system (CNS) cancer classification based on gene expression profiles

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Summary

Introduction

Cancer is a common disease caused by certain abnormal changes to genes that are responsible for cell division and growth. These recognizable changes include mutations of the DNA that make up genes. Cancer cells exhibit significantly more genetic changes than normal cells, cancerous tumours show different specific combinations of genetic alterations in different people. A few of these recognizable changes may be the result of the cancer rather than its cause. Developing appropriate methodologies that can effectively distinguish among tumour subtypes is vital. Diagnosis of cancer is essential for sufficient and effective treatment because every cancer type requires specific treatment

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