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开发并使用 Cytoscape 应用程序进行 GRNCOP2。

Development and use of a Cytoscape app for GRNCOP2.

机构信息

Intelligent Data Analysis (DATAi), Division of Computer Science, Pablo de Olavide University, Seville ES-41013, Spain.

Instituto de Ciencias e Ingeniería de la Computaciǿn (UNS, CONICET), Departamento de Ciencias e Ingeniería de la Computaciǿn, Universidad Nacional del Sur (UNS), Bahía Blanca, Argentina.

出版信息

Comput Methods Programs Biomed. 2019 Aug;177:211-218. doi: 10.1016/j.cmpb.2019.05.030. Epub 2019 Jun 4.

Abstract

BACKGROUND AND OBJECTIVE

Gene regulatory networks (GRNs) are essential for understanding most molecular processes. In this context, the so-called model-free approaches have an advantage modeling the complex topologies behind these dynamic molecular networks, since most GRNs are difficult to map correctly by any other mathematical model. Abstract model-free approaches, also known as rule-based extraction methods, offer valuable benefits when performing data-driven analysis; such as requiring the least amount of data and simplifying the inference of large models at a faster analysis speed. In particular, GRNCOP2 is a combinatorial optimization method with an adaptive criterion for the discretization of gene expression data and high performance, in contrast to other rule-based extraction methods for discovering GRNs. However, the analysis of the large relational structures of the networks inferred by GRNCOP2 requires the support of effective tools for interactive network visualization and topological analysis of the extracted associations. This need motivated the possibility of integrating GRNCOP2 in the Cytoscape ecosystem in order to benefit from Cytoscapes core functionality, as well as all the other apps in its ecosystem.

METHODS

In this paper, we introduce the implementation of a GRNCOP2 Cytoscape app. This incorporation to Cytoscape platform includes new functionality for GRN visualizations, dynamic user-interaction and integration with other apps for topological analysis of the networks.

RESULTS

In order to demonstrate the usefulness of integrating GRNCOP2 in Cytoscape, the new app was used to tackle a novel use case for GRNCOP2: the analysis of crosstalk between pathways. In this regard, datasets associated with Alzheimer's disease (AD) were analyzed using GRNCOP2 app and other apps of the Cytoscape ecosystem by performing a topological analysis of the AD progression and its synchronization with the Ubiquitin Mediated Proteolysis pathway. Finally, the biological relevance of the findings achieved by this new app were evaluated by searching for evidence in the literature.

CONCLUSIONS

The proposed crosstalk analysis with the new GRNCOP2 app focused on assessing the phase of the Alzheimer's disease progression where the coordination with the Ubiquitin Mediated Proteolysis pathway increase, and identifying the genes that explain the signalling between these cellular processes. Both questions were explored by topological contrastive analysis of the GRNs generated for the GRNCOP2 app, where several facilities of Cytoscape were exploited. The topological patterns inferred by this new App have been consistent with biological evidence reported in the scientic literature, illustrating the effectiveness of using this new GRNCOP2 App in pathway analysis.

AVAILABILITY

The GRNCOP2 App is freely available at the official Cytoscape app store: http://apps.cytoscape.org/apps/grncop2.

摘要

背景与目的

基因调控网络(GRNs)对于理解大多数分子过程至关重要。在这种情况下,所谓的无模型方法在对这些动态分子网络背后的复杂拓扑结构进行建模方面具有优势,因为大多数 GRNs 很难通过任何其他数学模型正确映射。无模型方法,也称为基于规则的提取方法,在执行数据驱动分析时具有宝贵的优势,例如需要最少的数据量,并以更快的分析速度简化对大型模型的推断。特别是,GRNCOP2 是一种组合优化方法,具有用于基因表达数据离散化的自适应标准,与其他用于发现 GRNs 的基于规则的提取方法相比具有高性能。然而,对 GRNCOP2 推断的网络的大关系结构的分析需要有效的工具来支持交互式网络可视化和提取关联的拓扑分析。这种需求促使将 GRNCOP2 集成到 Cytoscape 生态系统中成为可能,以便从 Cytoscape 的核心功能以及其生态系统中的所有其他应用程序中受益。

方法

在本文中,我们介绍了 GRNCOP2 Cytoscape 应用程序的实现。这种对 Cytoscape 平台的集成包括用于 GRN 可视化、动态用户交互以及与用于网络拓扑分析的其他应用程序集成的新功能。

结果

为了展示将 GRNCOP2 集成到 Cytoscape 中的有用性,使用新应用程序解决了 GRNCOP2 的一个新用例:分析途径之间的串扰。在这方面,通过对阿尔茨海默病(AD)相关数据集进行分析,使用 GRNCOP2 应用程序和 Cytoscape 生态系统中的其他应用程序对 AD 进展及其与泛素介导的蛋白水解途径的同步进行拓扑分析。最后,通过在文献中搜索证据来评估通过这个新应用程序获得的发现的生物学相关性。

结论

使用新的 GRNCOP2 应用程序进行的拟议串扰分析侧重于评估与泛素介导的蛋白水解途径协调增加的阿尔茨海默病进展阶段,并确定解释这些细胞过程之间信号的基因。这两个问题都是通过对 GRNCOP2 应用程序生成的 GRNs 进行拓扑对比分析来探索的,其中利用了 Cytoscape 的多个功能。通过该新应用程序推断出的拓扑模式与科学文献中报道的生物学证据一致,说明了在途径分析中使用此新的 GRNCOP2 应用程序的有效性。

可用性

GRNCOP2 应用程序可在官方 Cytoscape 应用程序商店免费获得:http://apps.cytoscape.org/apps/grncop2。

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