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Inferring data-specific micro-RNA function through the joint ranking of micro-RNA and pathways from matched micro-RNA and gene expression data

机译:通过联合对微RNA的排名以及来自匹配微RNA和基因表达数据的途径来推断数据特定的微RNA功能

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摘要

>Motivation: In practice, identifying and interpreting the functional impacts of the regulatory relationships between micro-RNA and messenger-RNA is non-trivial. The sheer scale of possible micro-RNA and messenger-RNA interactions can make the interpretation of results difficult.>Results: We propose a supervised framework, pMim, built upon concepts of significance combination, for jointly ranking regulatory micro-RNA and their potential functional impacts with respect to a condition of interest. Here, pMim directly tests if a micro-RNA is differentially expressed and if its predicted targets, which lie in a common biological pathway, have changed in the opposite direction. We leverage the information within existing micro-RNA target and pathway databases to stabilize the estimation and annotation of micro-RNA regulation making our approach suitable for datasets with small sample sizes. In addition to outputting meaningful and interpretable results, we demonstrate in a variety of datasets that the micro-RNA identified by pMim, in comparison to simpler existing approaches, are also more concordant with what is described in the literature.>Availability and implementation: This framework is implemented as an >R function, pMim, in the package sydSeq available from .>Contact: >Supplementary information: are available at Bioinformatics online.
机译:>动机:在实践中,识别和解释微RNA与信使RNA之间调节关系的功能影响并非易事。可能的微小RNA和信使RNA相互作用的绝对规模会使结果难以解释。>结果:我们提出了一种基于重要性组合概念的监督框架pMim,用于联合排名监管微观-RNA及其对相关疾病的潜在功能影响。在这里,pMim直接测试微RNA是否差异表达,以及其位于共同生物学途径中的预测靶标是否已朝相反方向变化。我们利用现有微RNA靶标和途径数据库中的信息来稳定微RNA调控的估计和注释,从而使我们的方法适用于小样本数据集。除了输出有意义和可解释的结果外,我们还在各种数据集中证明了与简单的现有方法相比,pMim鉴定的微小RNA也与文献中描述的更为一致。>可用性和实现::此框架以sydSeq包中的> R 函数pMim的形式提供。>联系人: >补充信息:可在生物信息学在线获得。

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