LifeGlimmer GmbH, Markelstrasse 38, 12163, Berlin, Germany.
Laboratory of Systems and Synthetic Biology, Wageningen University & Research, Stippeneng 4, 6708 WE, Wageningen, The Netherlands.
BMC Bioinformatics. 2018 Nov 6;19(1):403. doi: 10.1186/s12859-018-2426-5.
Systems biology takes a holistic approach by handling biomolecules and their interactions as big systems. Network based approach has emerged as a natural way to model these systems with the idea of representing biomolecules as nodes and their interactions as edges. Very often the input data come from various sorts of omics analyses. Those resulting networks sometimes describe a wide range of aspects, for example different experiment conditions, species, tissue types, stimulating factors, mutants, or simply distinct interaction features of the same network produced by different algorithms. For these scenarios, synchronous visualization of more than one distinct network is an excellent mean to explore all the relevant networks efficiently. In addition, complementary analysis methods are needed and they should work in a workflow manner in order to gain maximal biological insights.
In order to address the aforementioned needs, we have developed a Synchronous Network Data Integration (SyNDI) framework. This framework contains SyncVis, a Cytoscape application for user-friendly synchronous and simultaneous visualization of multiple biological networks, and it is seamlessly integrated with other bioinformatics tools via the Galaxy platform. We demonstrated the functionality and usability of the framework with three biological examples - we analyzed the distinct connectivity of plasma metabolites in networks associated with high or low latent cardiovascular disease risk; deeper insights were obtained from a few similar inflammatory response pathways in Staphylococcus aureus infection common to human and mouse; and regulatory motifs which have not been reported associated with transcriptional adaptations of Mycobacterium tuberculosis were identified.
Our SyNDI framework couples synchronous network visualization seamlessly with additional bioinformatics tools. The user can easily tailor the framework for his/her needs by adding new tools and datasets to the Galaxy platform.
系统生物学采用整体方法,将生物分子及其相互作用视为大系统。基于网络的方法已成为一种自然的方式来对这些系统建模,其想法是将生物分子表示为节点,将它们的相互作用表示为边。输入数据通常来自各种组学分析。这些生成的网络有时描述了广泛的方面,例如不同的实验条件、物种、组织类型、刺激因素、突变体,或者只是由不同算法产生的相同网络的不同相互作用特征。对于这些情况,同时可视化多个不同的网络是高效探索所有相关网络的绝佳手段。此外,还需要互补的分析方法,并且它们应该以工作流程的方式工作,以获得最大的生物学见解。
为了满足上述需求,我们开发了一个同步网络数据集成(SyNDI)框架。该框架包含 SyncVis,这是一个 Cytoscape 应用程序,用于用户友好地同时可视化多个生物网络,并且通过 Galaxy 平台与其他生物信息学工具无缝集成。我们用三个生物学示例演示了框架的功能和可用性——我们分析了与高或低潜在心血管疾病风险相关的网络中血浆代谢物的不同连通性;从金黄色葡萄球菌感染中几个类似的炎症反应途径中获得了更深入的见解,这些途径在人类和小鼠中很常见;并且鉴定了与结核分枝杆菌转录适应性相关但尚未报道的调节基序。
我们的 SyNDI 框架将同步网络可视化与其他生物信息学工具无缝结合。用户可以通过向 Galaxy 平台添加新工具和数据集轻松地根据自己的需求定制框架。