Contextual Hub Analysis Tool (CHAT): A Cytoscape app for identifying contextually relevant hubs in biological networks.

Q2 Pharmacology, Toxicology and Pharmaceutics F1000Research Pub Date : 2016-01-01 DOI:10.12688/F1000RESEARCH.9118.1
Tanja Muetze, Ivan H. Goenawan, H. Wiencko, Manuel Bernal-Llinares, K. Bryan, D. Lynn
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引用次数: 17

Abstract

Highly connected nodes (hubs) in biological networks are topologically important to the structure of the network and have also been shown to be preferentially associated with a range of phenotypes of interest. The relative importance of a hub node, however, can change depending on the biological context. Here, we report a Cytoscape app, the Contextual Hub Analysis Tool (CHAT), which enables users to easily construct and visualize a network of interactions from a gene or protein list of interest, integrate contextual information, such as gene expression or mass spectrometry data, and identify hub nodes that are more highly connected to contextual nodes (e.g. genes or proteins that are differentially expressed) than expected by chance. In a case study, we use CHAT to construct a network of genes that are differentially expressed in Dengue fever, a viral infection. CHAT was used to identify and compare contextual and degree-based hubs in this network. The top 20 degree-based hubs were enriched in pathways related to the cell cycle and cancer, which is likely due to the fact that proteins involved in these processes tend to be highly connected in general. In comparison, the top 20 contextual hubs were enriched in pathways commonly observed in a viral infection including pathways related to the immune response to viral infection. This analysis shows that such contextual hubs are considerably more biologically relevant than degree-based hubs and that analyses which rely on the identification of hubs solely based on their connectivity may be biased towards nodes that are highly connected in general rather than in the specific context of interest. AVAILABILITY CHAT is available for Cytoscape 3.0+ and can be installed via the Cytoscape App Store ( http://apps.cytoscape.org/apps/chat).
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上下文枢纽分析工具(CHAT):一个用于识别生物网络中上下文相关枢纽的Cytoscape应用程序。
生物网络中高度连接的节点(枢纽)在拓扑结构上对网络结构很重要,并且也被证明优先与一系列感兴趣的表型相关。然而,枢纽节点的相对重要性可以根据生物环境而改变。在这里,我们报告了一个Cytoscape应用程序,上下文枢纽分析工具(CHAT),它使用户能够轻松地从感兴趣的基因或蛋白质列表中构建和可视化交互网络,整合上下文信息,如基因表达或质谱数据,并识别与上下文节点(例如差异表达的基因或蛋白质)联系更紧密的枢纽节点。在一个案例研究中,我们使用CHAT构建了一个在登革热病毒感染中差异表达的基因网络。CHAT用于识别和比较该网络中基于上下文和学位的中心。前20个基于学位的中心在与细胞周期和癌症相关的途径中富集,这可能是由于参与这些过程的蛋白质通常是高度相关的。相比之下,前20个上下文枢纽在病毒感染中通常观察到的途径中富集,包括与病毒感染免疫反应相关的途径。这一分析表明,与基于学位的枢纽相比,这种上下文枢纽在生物学上的相关性要高得多,而仅仅依赖于基于连接性来识别枢纽的分析可能会偏向于一般高度连接的节点,而不是特定的感兴趣背景。AVAILABILITYCHAT适用于Cytoscape 3.0+,可以通过Cytoscape应用商店(http://apps.cytoscape.org/apps/chat)安装。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
F1000Research
F1000Research Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.00
自引率
0.00%
发文量
1646
审稿时长
1 weeks
期刊介绍: F1000Research publishes articles and other research outputs reporting basic scientific, scholarly, translational and clinical research across the physical and life sciences, engineering, medicine, social sciences and humanities. F1000Research is a scholarly publication platform set up for the scientific, scholarly and medical research community; each article has at least one author who is a qualified researcher, scholar or clinician actively working in their speciality and who has made a key contribution to the article. Articles must be original (not duplications). All research is suitable irrespective of the perceived level of interest or novelty; we welcome confirmatory and negative results, as well as null studies. F1000Research publishes different type of research, including clinical trials, systematic reviews, software tools, method articles, and many others. Reviews and Opinion articles providing a balanced and comprehensive overview of the latest discoveries in a particular field, or presenting a personal perspective on recent developments, are also welcome. See the full list of article types we accept for more information.
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