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首页> 外文期刊>Pattern Recognition: The Journal of the Pattern Recognition Society >A new framework for identifying differentially expressed genes
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A new framework for identifying differentially expressed genes

机译:鉴定差异表达基因的新框架

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摘要

Microarrays have been widely used to classify cancer samples and discover the biological types, for example tumor versus normal phenotypes in cancer research. One of the challenging scientific tasks in the post-genomic epoch is how to identify a subset of differentially expressed genes from thousands of genes in microarray data which will enable us to understand the underlying molecular mechanisms of diseases, accurately diagnosing diseases and identifying novel therapeutic targets. In this paper, we propose a new framework for identifying differentially expressed genes. In the proposed framework, genes are ranked according to their residuals. The performance of the framework is assessed through applying it to several public microarray data. Experimental results show that the proposed method gives more robust and accurate rank than other statistical test methods, such as t-test, Wilcoxon rank sum test and KS-test. Another novelty of the method is that we design an algorithm for selecting a small subset of genes that show significant variation in expression ("outlier" genes). The number of genes in the small subset can be controlled via an alterable window of confidence level. In addition, the results of the proposed method can be visualized. By observing the residual plot, we can easily find genes that show significant variation in two groups of samples and learn the degrees of differential expression of genes. Through a comparison study, we found several "outlier" genes which had been verified in previous biological experiments while they were either not identified by other methods or had lower ranks in standard statistical tests. (c) 2007 Pattern Recognition Society. Published by Elsevier Ltd. All rights reserved.
机译:微阵列已被广泛用于癌症样品的分类并发现生物学类型,例如癌症研究中的肿瘤与正常表型。基因组后时代的挑战性科学任务之一是如何从微阵列数据中的数千个基因中鉴定差异表达基因的子集,这将使我们能够了解疾病的潜在分子机制,准确诊断疾病并确定新的治疗靶点。在本文中,我们提出了鉴定差异表达基因的新框架。在提出的框架中,基因根据其残基进行排序。该框架的性能通过将其应用于多个公共微阵列数据进行评估。实验结果表明,与t检验,Wilcoxon秩和检验和KS检验等其他统计检验方法相比,该方法具有更高的鲁棒性和准确性。该方法的另一个新颖之处在于,我们设计了一种算法,用于选择一小部分表现出表达差异的基因(“异常”基因)。小子集中的基因数量可以通过置信度水平的可变窗口来控制。另外,所提出的方法的结果可以被可视化。通过观察残差图,我们可以轻松地找到在两组样本中显示出显着差异的基因,并了解基因的差异表达程度。通过比较研究,我们发现了几个“异常”基因,这些基因在先前的生物学实验中得到了验证,而这些基因要么无法通过其他方法进行鉴定,要么在标准统计测试中的排名较低。 (c)2007模式识别学会。由Elsevier Ltd.出版。保留所有权利。

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