Applications that classify DNA microarray expression data are helpful for diagnosing cancer. Many attempts have been made to analyze these data; however, new methods are needed to obtain better results. In this study, a Complex Network (CN) classifier was exploited to implement the classification task. An algorithm was used to initialize the structure, which allowed input variables to be selected over layered connections and different activation functions for different nodes. Then, a hybrid method integrated the Genetic Programming and the Particle Swarm Optimization algorithms was used to identify an optimal structure with the parameters encoded in the classifier. The single CN classifier and an ensemble of CN classifiers were tested on four bench data sets. To ensure diversity of the ensemble classifiers, we constructed a base classifier using different feature sets, i.e., Pearson's correlation, Spearman's correlation, Euclidean distance, Cosine coefficient and the Fisher-ratio. The experimental results suggest that a single classifier can be used to obtain state-of-the-art results and the ensemble yielded better results.

BACKGROUND: For a protein to execute its function, ensuring its correct subcellular localization is essential. In addition to biological experiments, bioinformatics is widely used to predict and determine the subcellular localization of proteins. However, single-feature extraction methods cannot effectively handle the huge amount of data and multisite localization of proteins. Thus, we developed a pseudo amino acid composition (PseAAC) method and an entropy density technique to extract feature fusion information from subcellular multisite proteins. OBJECTIVE: Predicting multiplex protein subcellular localization and achieve high prediction accuracy. METHOD: To improve the efficiency of predicting multiplex protein subcellular localization, we used the multi-label k-nearest neighbors algorithm and assigned different weights to various attributes. The method was evaluated using several performance metrics with a dataset consisting of protein sequences with single-site and multisite subcellular localizations. RESULTS: Evaluation experiments showed that the proposed method significantly improves the optimal overall accuracy rate of multiplex protein subcellular localization. CONCLUSION: This method can help to more comprehensively predict protein subcellular localization toward better understanding protein function, thereby bridging the gap between theory and application toward improved identification and monitoring of drug targets.