A novel filter feature selection method for paired microarray expression data analysis.

Pub Date : 2015-01-01 DOI:10.1504/ijdmb.2015.070071
Zhongbo Cao, Yan Wang, Ying Sun, Wei Du, Yanchun Liang
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引用次数: 13

Abstract

In recent years, a large amount of microarray data sets are produced with tens of thousands of genes. Feature selection has become a very sharp tool to select the informative genes. However, few feature selection methods consider the effect of paired samples, which are much more considered in the experiments of these years. Here, we propose a new feature selection method for paired microarray data sets analysis. It uses the fold change instead of the subtraction in the original approach, measures the statistical significant using the q-value of False Discovery Rate (FDR) and also decreases the influence of redundant genes. We compare the proposed method with another six existing methods in predict performance, stability of gene lists, functional stability and functional enrichment analysis using six kinds of paired cancer data sets. Comparison results show that our proposed method achieves better effectiveness, stability and consistency when it is applied to paired data sets.

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一种新的滤波特征选择方法用于配对微阵列表达数据分析。
近年来,数以万计的基因产生了大量的微阵列数据集。特征选择已经成为选择信息基因的一种非常锐利的工具。然而,很少有特征选择方法考虑到配对样本的影响,而这在近年来的实验中得到了更多的考虑。在此,我们提出了一种新的特征选择方法用于配对微阵列数据集分析。该方法采用折叠变化代替原方法中的减法,使用错误发现率(FDR)的q值来衡量统计显著性,并降低冗余基因的影响。我们使用6种配对的癌症数据集,将所提出的方法与其他6种现有方法在预测性能、基因列表稳定性、功能稳定性和功能富集分析方面进行了比较。对比结果表明,该方法在应用于成对数据集时具有更好的有效性、稳定性和一致性。
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