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Identification genes of colorectal cancer with integrated data via Block-sparse NMFL21

机译:通过块稀疏NMFL21鉴定与集成数据结直肠癌的鉴定基因

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Colorectal cancer is the second leading cause of cancer deaths in the word. The assessment of the colorectal cancer is determined by the clinical stage which denotes the number of lymph nodes with metastatic cancer and the identification of metastatic sites in other organs. While the cancer genes associated with colorectal cancer have been characterized, less is known about the identity of special cancer genes that are responsible for advanced clinical stage and metastasis. To characterize genetic aberration in colorectal cancer, we conducted a Block-sparse nonnegative matrix factorization with L_(2l) -norm (Block-sparse NMF L_(21)) analysis of multiple genomic data which include mutation, DNA copy number, promoter methylation, messenger RNA and microRNA expression from The Cancer Genome Atlas (TCGA). With the analysis of the method, we ranked the genes by the scores and identified a set of top gene predictors of advanced clinical stage. The results demonstrate that the analysis of integrated data through block-sparse NMF L_(21) is more comprehensive.
机译:结肠直肠癌是癌症死亡的第二个主要原因。结直肠癌的评估由临床阶段确定,临床阶段表示具有转移性癌症的淋巴结数和其他器官中的转移性位点。虽然已经表征了与结肠直肠癌相关的癌症基因,但较少关于对晚期临床阶段和转移的特殊癌症基因的身份而闻名。为了表征结直肠癌中的遗传像差,我们用L_(2L)-NOMM进行嵌段稀疏的非负基质分子,(块状NMF L_(21))分析多种基因组数据,包括突变,DNA拷贝数,启动子甲基化,来自癌症基因组Atlas(TCGA)的信使RNA和MicroRNA表达。随着该方法的分析,我们通过评分排名基因并鉴定了一组高级临床阶段的顶部基因预测因子。结果表明,通过块稀疏NMF L_(21)分析集成数据更全面。

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