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SIMILARITIES OF ORDERED GENE LISTS

机译:有序基因清单的相似性

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Motivation: Many applications of microarray technology in clinical cancer studies aim at detecting molecular features for refined diagnosis. In this paper, we follow an opposite rationale: we try to identify common molecular features shared by phenotypically distinct types of cancer using a meta-analysis of several microarray studies. We present a novel algorithm to uncover that two lists of differentially expressed genes are similar, even if these similarities are not apparent to the eye. The method is based on the ordering in the lists. Results: In a meta-analysis of five clinical microarray studies we were able to detect significant similarities in five of the ten possible comparisons of ordered gene lists. We included sUidies, where not a single gene can be significantly associated to outcome. The detection of significant similarities of gene lists from different microarray studies is a novel and promising approach. It has the potential to improve upon specialized cancer studies by exploring the power of several studies in one single analysis. Our method is complementary to previous methods in that it does not rely on strong effects of differential gene expression in a single study but on consistent ones across multiple studies.
机译:动机:微阵列技术在临床癌症研究中的许多应用旨在检测分子特征以进行精确诊断。在本文中,我们遵循相反的原理:我们通过对数个微阵列研究的荟萃分析,试图确定表型不同类型癌症共有的共同分子特征。我们提出了一种新颖的算法来揭示差异表达基因的两个列表是相似的,即使这些相似性在眼睛中并不明显。该方法基于列表中的顺序。结果:在对五项临床微阵列研究的荟萃分析中,我们能够在有序基因列表的十种可能比较中的五种中检测出显着相似性。我们纳入了研究,其中没有一个基因可以与结果显着相关。从不同的微阵列研究中检测基因列表的显着相似性是一种新颖且有希望的方法。通过在一项分析中探索多项研究的力量,它有可能改善专门的癌症研究。我们的方法是对先前方法的补充,因为它不依赖于单个研究中差异基因表达的强大影响,而是依赖于多个研究中一致的结果。

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