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代谢重建的计算方法。

Computational methods for metabolic reconstruction.

机构信息

Department of Computer Science, University of Helsinki, P.O. Box 68 (Gustaf Hällströmin katu 2b), 00014 Helsinki, Finland.

出版信息

Curr Opin Biotechnol. 2010 Feb;21(1):70-7. doi: 10.1016/j.copbio.2010.01.010. Epub 2010 Feb 18.

DOI:10.1016/j.copbio.2010.01.010
PMID:20171871
Abstract

In the wake of numerous sequenced genomes becoming available, computational methods for the reconstruction of metabolic networks have received considerable attention. Here, we review recent methods and software tools useful along the reconstruction workflow, from sequence annotation and network assembly to model verification and testing against experimental data. Reconstruction methods can be divided into three categories, depending on the magnitude of network context which is taken into account in the process of assembling the metabolic model: First, each enzyme may be predicted independently by annotation transfer or machine learning methods. Second, the presence of a metabolic pathway may be detected from genome and experimental evidence, often utilizing a reference pathway database. Third, the method may attempt to directly reconstruct a consistent metabolic network without relying on predefined reference pathways. Regardless of the chosen context, all methods strive to reconstruct genome-scale metabolic reconstructions. Currently a gap exists between software platforms dedicated to genome annotation and computational tools for automatically repairing network inconsistencies and validating against measurement data. We argue that to accelerate the reconstruction efforts, computational tools need to be developed that bridge the phases of the reconstruction workflow. In particular, the goal of finding consistent metabolic models suitable for computational analysis should be taken into account already in the beginning phases of reconstruction.

摘要

随着大量测序基因组的出现,用于重建代谢网络的计算方法受到了广泛关注。在这里,我们回顾了最近的方法和软件工具,这些方法和工具沿着重建工作流程是有用的,从序列注释和网络组装到模型验证和与实验数据的测试。重建方法可以根据在组装代谢模型过程中考虑的网络上下文的大小分为三类:首先,可以通过注释转移或机器学习方法独立预测每个酶。其次,可以从基因组和实验证据中检测到代谢途径的存在,通常利用参考途径数据库。第三,可以尝试直接重建一致的代谢网络,而不依赖于预定义的参考途径。无论选择何种上下文,所有方法都努力重建基因组规模的代谢重建。目前,专门用于基因组注释的软件平台和用于自动修复网络不一致性并针对测量数据进行验证的计算工具之间存在差距。我们认为,为了加快重建工作,需要开发计算工具来弥合重建工作流程的各个阶段。特别是,在重建的初始阶段就应该考虑到找到适合计算分析的一致代谢模型的目标。

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