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A fuzzy based feature selection from independent component subspace for machine learning classification of microarray data

机译:从独立分量子空间中基于模糊的特征选择用于微阵列数据的机器学习分类

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摘要

Feature (gene) selection and classification of microarray data are the two most interesting machine learning challenges. In the present work two existing feature selection/extraction algorithms, namely independent component analysis (ICA) and fuzzy backward feature elimination (FBFE) are used which is a new combination of selection/extraction. The main objective of this paper is to select the independent components of the DNA microarray data using FBFE to improve the performance of support vector machine (SVM) and Naïve Bayes (NB) classifier, while making the computational expenses affordable. To show the validity of the proposed method, it is applied to reduce the number of genes for five DNA microarray datasets namely; colon cancer, acute leukemia, prostate cancer, lung cancer II, and high-grade glioma. Now these datasets are then classified using SVM and NB classifiers. Experimental results on these five microarray datasets demonstrate that gene selected by proposed approach, effectively improve the performance of SVM and NB classifiers in terms of classification accuracy. We compare our proposed method with principal component analysis (PCA) as a standard extraction algorithm and find that the proposed method can obtain better classification accuracy, using SVM and NB classifiers with a smaller number of selected genes than the PCA. The curve between the average error rate and number of genes with each dataset represents the selection of required number of genes for the highest accuracy with our proposed method for both the classifiers. ROC shows best subset of genes for both the classifier of different datasets with propose method.
机译:微阵列数据的特征(基因)选择和分类是两个最有趣的机器学习挑战。在本工作中,使用了两个现有的特征选择/提取算法,即独立成分分析(ICA)和模糊后向特征消除(FBFE),这是选择/提取的新组合。本文的主要目的是使用FBFE选择DNA微阵列数据的独立组成部分,以提高支持向量机(SVM)和朴素贝叶斯(NB)分类器的性能,同时使计算费用负担得起。为了证明该方法的有效性,将其用于减少五个DNA微阵列数据集的基因数目。结肠癌,急性白血病,前列腺癌,肺癌II和高级别神经胶质瘤。现在,使用SVM和NB分类器对这些数据集进行分类。在这五个微阵列数据集上的实验结果表明,所提出的方法选择的基因在分类准确性方面有效地提高了SVM和NB分类器的性能。我们将本文提出的方法与主成分分析(PCA)作为标准提取算法进行比较,发现该方法与SPC和NB分类器相比,能够使用更好的分类准确率,并且选择的基因数量少于PCA。每个数据集的平均错误率和基因数量之间的曲线代表了我们针对两个分类器提出的方法所需要的基因数量,以实现最高的准确性。 ROC使用提议方法显示了不同数据集的两个分类器的最佳基因子集。

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