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通过利用局部多样性实现代谢途径的简单快速比对。

Simple and fast alignment of metabolic pathways by exploiting local diversity.

作者信息

Wernicke Sebastian, Rasche Florian

机构信息

Institut für Informatik, Friedrich-Schiller-Universität Jena, Jena, Germany.

出版信息

Bioinformatics. 2007 Aug 1;23(15):1978-85. doi: 10.1093/bioinformatics/btm279. Epub 2007 May 31.

Abstract

MOTIVATION

An important tool for analyzing biological networks is the ability to perform homology searches, i.e. given a pattern network one would like to be able to search for occurrences of similar (sub)networks within a set of host networks. In the context of metabolic pathways, Pinter et al. [Bioinformatics, 2005] proposed to solve this computationally hard problem by restricting it to the case where both the pattern and host networks are trees. This restriction, however, severely limits the applicability of their algorithm.

RESULTS

We propose a very fast and simple algorithm for the alignment of metabolic pathways that does not restrict the topology of the host or pattern network in any way; instead, our algorithm exploits a natural property of metabolic networks that we call 'local diversity property'. Experiments on a test bed of metabolic pathways from the BioCyc database indicate that our algorithm is much faster than the restricted algorithm of Pinter et al.-the metabolic pathways of two organisms can be aligned in mere seconds-and yet has a wider range of applicability and yields new biological insights. Our ideas can likely be extended to work for the alignment of various types of biological networks other than metabolic pathways.

AVAILABILITY

Our algorithm has been implemented in C++ as a user-friendly metabolic pathway alignment tool called METAPAT. The tool runs under Linux or Windows and can be downloaded at http://theinf1.informatik.uni-jena.de/metapat/

摘要

动机

分析生物网络的一个重要工具是进行同源性搜索的能力,即给定一个模式网络,希望能够在一组宿主网络中搜索相似(子)网络的出现情况。在代谢途径的背景下,平特等人[《生物信息学》,2005年]提议通过将其限制在模式网络和宿主网络均为树的情况来解决这个计算难题。然而,这种限制严重限制了他们算法的适用性。

结果

我们提出了一种非常快速且简单的代谢途径比对算法,该算法不以任何方式限制宿主或模式网络的拓扑结构;相反,我们的算法利用了代谢网络的一种自然属性,我们称之为“局部多样性属性”。在来自BioCyc数据库的代谢途径测试平台上进行的实验表明,我们的算法比平特等人的受限算法快得多——两种生物体的代谢途径只需几秒钟就能比对完成——而且具有更广泛的适用性,并能产生新的生物学见解。我们的想法很可能可以扩展到适用于除代谢途径之外的各种类型生物网络的比对。

可用性

我们的算法已用C++实现,作为一个名为METAPAT的用户友好型代谢途径比对工具。该工具可在Linux或Windows下运行,可从http://theinf1.informatik.uni-jena.de/metapat/下载。

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