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Tensor decomposition-based unsupervised feature extraction for integrated analysis of TCGA data on microRNA expression and promoter methylation of genes in ovarian cancer

机译:基于张量分解的无预测特征提取,用于卵巢癌中基因TCGA数据综合分析及卵巢癌基因的促进剂甲基化

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Integrated analysis of epigenetic profiles is important but difficult. Tensor decomposition-based unsupervised feature extraction was applied here to data on microRNA (miRNA) expression and promoter methylation of genes in ovarian cancer. It selected seven miRNAs and 241 genes by expression levels and promoter methylation degrees, respectively, such that they showed differences between eight normal ovarian tissue samples and 569 tumor samples. The expression levels of the seven miRNAs and the degrees of promoter methylation of the 241 genes also correlated significantly. Conventional Student's t test-based feature selection failed to identify miRNAs and genes that have the above properties. On the other hand, biological evaluation of the seven identified miRNAs and 241 identified genes suggests that they are strongly related to cancer as expected.
机译:表观遗传型材的综合分析很重要,但困难。将张量分解的无预测特征提取应用于微小RNA(miRNA)表达和卵巢癌中基因的启动子甲基化的数据。它通过表达水平和启动子甲基化度分别选择了七个miRNA和241个基因,使得它们在八个正常卵巢组织样品和569个肿瘤样品之间显示出差异。七个miRNA的表达水平和241个基因的促进剂甲基化也显着相关。传统的学生的T基于T测试的特征选择未能识别具有上述性质的miRNA和基因。另一方面,七种鉴定的miRNA和241个鉴定基因的生物学评估表明它们与预期的癌症密切相关。

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