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BIOMARKER DISCOVERY AND VISUALIZATION IN GENE EXPRESSION DATA WITH EFFICIENT GENERALIZED MATRIX APPROXIMATIONS

机译:基因表达数据中生物标记的发现和可视化及其有效的矩阵近似

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摘要

In most real-world gene expression data sets, there are often multiple sample classes with ordinals, which are categorized into the normal or diseased type. The traditional feature or attribute selection methods consider multiple classes equally without paying attention to the up/down regulation across the normal and diseased types of classes, while the specific gene selection methods particularly consider the differential expressions across the normal and diseased, but ignore the existence of multiple classes. In this paper, to improve the biomarker discovery, we propose to make the best use of these two aspects: the differential expressions (that can be viewed as the domain knowledge of gene expression data) and the multiple classes (that can be viewed as a kind of data set characteristic). Therefore, we simultaneously take into account these two aspects by employing the 1-rank generalized matrix approximations (GMA). Our results show that GMA cannot only improve the accuracy of classifying the samples, but also provide a visualization method to effectively analyze the gene expression data on both genes and samples. Based on the mechanism of matrix approximation, we further propose an algorithm, CBiomarker, to discover compact biomarker by reducing the redundancy.
机译:在大多数现实世界的基因表达数据集中,通常有多个带有普通样本的样本类别,这些样本类别被分为正常或患病类型。传统的特征或属性选择方法平等地考虑多个类别,而不关注正常和患病类型的上/下调节,而特定的基因选择方法特别考虑了正常和患病类型的差异表达,但忽略了存在多类。在本文中,为了改善生物标志物的发现,我们建议充分利用这两个方面:差异表达(可以看作是基因表达数据的领域知识)和多个类别(可以看作是基因表达数据的领域知识)。一种数据集特征)。因此,我们通过采用1级广义矩阵逼近(GMA)同时考虑到这两个方面。我们的结果表明,GMA不仅可以提高样本分类的准确性,而且还提供了一种可视化方法,可以有效地分析基因和样本上的基因表达数据。基于矩阵逼近的机制,我们进一步提出了一种算法CBiomarker,通过减少冗余来发现紧凑的生物标记。

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