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ChainRank, a chain prioritisation method for contextualisation of biological networks

机译:ChainRank,一种用于生物网络环境的链优先化方法

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Advances in high throughput technologies and growth of biomedical knowledge have contributed to an exponential increase in associative data. These data can be represented in the form of complex networks of biological associations, which are suitable for systems analyses. However, these networks usually lack both, context specificity in time and space as well as the distinctive borders, which are usually assigned in the classical pathway view of molecular events (e.g. signal transduction). This complexity and high interconnectedness call for automated techniques that can identify smaller targeted subnetworks specific to a given research context (e.g. a disease scenario). Our method, named ChainRank, finds relevant subnetworks by identifying and scoring chains of interactions that link specific network components. Scores can be generated from integrating multiple general and context specific measures (e.g. experimental molecular data from expression to proteomics and metabolomics, literature evidence, network topology). The performance of the novel ChainRank method was evaluated on recreating selected signalling pathways from a human protein interaction network. Specifically, we recreated skeletal muscle specific signaling networks in healthy and chronic obstructive pulmonary disease (COPD) contexts. The analysis showed that ChainRank can identify main mediators of context specific molecular signalling. An improvement of up to factor 2.5 was shown in the precision of finding proteins of the recreated pathways compared to random simulation. ChainRank provides a framework, which can integrate several user-defined scores and evaluate their combined effect on ranking interaction chains linking input data sets. It can be used to contextualise networks, identify signaling and regulatory path amongst targeted genes or to analyse synthetic lethality in the context of anticancer therapy. ChainRank is implemented in R programming language and freely available at https://github.com/atenyi/ChainRank .
机译:高通量技术的进步和生物医学知识的增长推动了关联数据的指数增长。这些数据可以以生物学关联的复杂网络的形式表示,适用于系统分析。然而,这些网络通常既缺乏时间和空间方面的背景特异性,又缺乏独特的边界,这通常是在分子事件的经典途径(例如信号转导)中分配的。这种复杂性和高度互连性要求采用自动化技术,该技术可以识别特定于给定研究环境(例如疾病情况)的较小目标子网。我们的名为ChainRank的方法通过识别和评分链接特定网络组件的交互链来找到相关的子网。可以通过整合多种常规和特定于情境的指标来生成分数(例如,从表达到蛋白质组学和代谢组学的实验分子数据,文献证据,网络拓扑)。通过从人蛋白质相互作用网络重建选定的信号通路,评估了新型ChainRank方法的性能。具体来说,我们在健康和慢性阻塞性肺疾病(COPD)的环境中重建了骨骼肌特异性信号网络。分析表明,ChainRank可以识别上下文相关分子信号的主要介体。与随机模拟相比,在找到重新创建的路径的蛋白质的精度上显示了高达2.5的改进。 ChainRank提供了一个框架,该框架可以集成多个用户定义的分数并评估它们对链接输入数据集的交互链的排名的综合影响。它可以用于关联网络,识别目标基因之间的信号传导和调控路径,或用于抗癌治疗中的合成杀伤力分析。 ChainRank以R编程语言实现,可从https://github.com/atenyi/ChainRank免费获得。

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