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PATHLOGIC-S:用于建模细胞信号的可扩展布尔框架。

PATHLOGIC-S: a scalable Boolean framework for modelling cellular signalling.

机构信息

Australian Institute of Bioengineering and Nanotechnology, University of Queensland, Brisbane, Queensland, Australia.

出版信息

PLoS One. 2012;7(8):e41977. doi: 10.1371/journal.pone.0041977. Epub 2012 Aug 7.

Abstract

Curated databases of signal transduction have grown to describe several thousand reactions, and efficient use of these data requires the development of modelling tools to elucidate and explore system properties. We present PATHLOGIC-S, a Boolean specification for a signalling model, with its associated GPL-licensed implementation using integer programming techniques. The PATHLOGIC-S specification has been designed to function on current desktop workstations, and is capable of providing analyses on some of the largest currently available datasets through use of Boolean modelling techniques to generate predictions of stable and semi-stable network states from data in community file formats. PATHLOGIC-S also addresses major problems associated with the presence and modelling of inhibition in Boolean systems, and reduces logical incoherence due to common inhibitory mechanisms in signalling systems. We apply this approach to signal transduction networks including Reactome and two pathways from the Panther Pathways database, and present the results of computations on each along with a discussion of execution time. A software implementation of the framework and model is freely available under a GPL license.

摘要

信号转导的精选数据库已发展到描述数千种反应,而要有效利用这些数据,则需要开发建模工具来阐明和探索系统特性。我们提出了 PATHLOGIC-S,这是一种用于信号模型的布尔规范,以及使用整数编程技术的相关 GPL 许可实现。PATHLOGIC-S 规范旨在在当前的台式工作站上运行,并且能够通过使用布尔建模技术从社区文件格式中的数据生成稳定和半稳定网络状态的预测,从而对当前可用的最大数据集之一进行分析。PATHLOGIC-S 还解决了与布尔系统中抑制作用的存在和建模相关的主要问题,并减少了由于信号系统中常见的抑制机制而导致的逻辑不连贯性。我们将这种方法应用于信号转导网络,包括 Reactome 和 Panther Pathways 数据库中的两个途径,并展示了对每个途径进行计算的结果,并讨论了执行时间。该框架和模型的软件实现可根据 GPL 许可证免费获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7fc/3413702/711ea285fa36/pone.0041977.g001.jpg

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