Abstract

The classification of tumors is crucial for the proper treatment of cancer. Sparse representation-based classifier (SRC) exhibits good classification performance and has been successfully used to classify tumors using gene expression profile data. In this study, we propose a three-step maxdenominator reweighted sparse representation classification (MRSRC) method to classify tumors. First, we extract a set of metagenes from the training samples. These metagenes can capture the structures inherent to the data and are more effective for classification than the original gene expression data. Second, we use a reweighted regularization method to obtain the sparse representation coefficients. Reweighted regularization can enhance sparsity and obtain better sparse representation coefficients. Third, we classify the data by utilizing a maxdenominator residual error function. Maxdenominator strategy can reduce the residual error and improve the accuracy of the final classification. Extensive experiments using publicly available gene expression profile data sets show that the performance of MRSRC is comparable with or better than many existing representative methods.

Highlights

  • Accurate tumor classification is beneficial for cancer treatment

  • singular value decomposition (SVD) was applied to capture the weighted metagenes[18], the test sample is represented as the linear combination of these weighted metagenes

  • These analytical results show that using metagenes to replace gene expression data can produce better results for classification

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Summary

Introduction

Accurate tumor classification is beneficial for cancer treatment. A tumor can be classified as benign, premalignant, or malignant, of which only a malignant tumor can be called cancer. A 1 norm least square method[12] is applied to search for the sparse representation coefficient which will decide the type of the test sample. We propose a maxdenominator residual error function which takes full advantage of the linear relation between test sample and metagenes to capture the classification from the sparse representation coefficients.

Results
Conclusion

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