首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Variable selection using probability density function similarity for support vector machine classification of high-dimensional microarray data
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Variable selection using probability density function similarity for support vector machine classification of high-dimensional microarray data

机译:使用概率密度函数相似度进行变量选择以对高维微阵列数据进行支持向量机分类

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摘要

One problem with discriminant analysis of microarray data is representation of each sample by a largenumber of genes that are possibly irrelevant, insignificant or redundant. Methods of variable selection are,therefore, of great significance in microarray data analysis. To circumvent the problem, a new gene miningapproach is proposed based on the similarity between probability density functions on each gene for theclass of interest with respect to the others. This method allows the ascertainment of significant genesthat are informative for discriminating each individual class rather than maximizing the separability ofall classes. Then one can select genes containing important information about the particular subtypes ofdiseases. Based on the mined significant genes for individual classes, a support vector machine with localkernel transform is constructed for the classification of different diseases. The combination of the genemining approach with support vector machine is demonstrated for cancer classification using two publicdata sets. The results reveal that significant genes are identified for each cancer, and the classificationmodel shows satisfactory performance in training and prediction for both data sets.
机译:微阵列数据的判别分析的一个问题是,每个样品由大量可能无关,无关紧要或多余的基因表示。因此,变量选择方法在微阵列数据分析中具有重要意义。为了解决这个问题,针对每个感兴趣类别的每个基因的概率密度函数之间的相似性,提出了一种新的基因挖掘方法。该方法可以确定重要的基因,这些基因可用于区分每个类别,而不是最大化所有类别的可分离性。然后,可以选择包含有关特定疾病亚型的重要信息的基因。基于各个类别的重要基因,构建了带有局部核转化的支持向量机,用于不同疾病的分类。使用两个公共数据集证明了将基因挖掘方法与支持向量机相结合用于癌症分类。结果表明,已为每种癌症鉴定出重要的基因,并且分类模型在两个数据集的训练和预测中均显示出令人满意的性能。

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