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多个数据源的综合分析揭示了生物网络的模块化结构。

Integrated analysis of multiple data sources reveals modular structure of biological networks.

作者信息

Lu Hongchao, Shi Baochen, Wu Gaowei, Zhang Yong, Zhu Xiaopeng, Zhang Zhihua, Liu Changning, Zhao Yi, Wu Tao, Wang Jie, Chen Runsheng

机构信息

Bioinformatics Laboratory and National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, PR China.

出版信息

Biochem Biophys Res Commun. 2006 Jun 23;345(1):302-9. doi: 10.1016/j.bbrc.2006.04.088. Epub 2006 Apr 27.

Abstract

It has been a challenging task to integrate high-throughput data into investigations of the systematic and dynamic organization of biological networks. Here, we presented a simple hierarchical clustering algorithm that goes a long way to achieve this aim. Our method effectively reveals the modular structure of the yeast protein-protein interaction network and distinguishes protein complexes from functional modules by integrating high-throughput protein-protein interaction data with the added subcellular localization and expression profile data. Furthermore, we take advantage of the detected modules to provide a reliably functional context for the uncharacterized components within modules. On the other hand, the integration of various protein-protein association information makes our method robust to false-positives, especially for derived protein complexes. More importantly, this simple method can be extended naturally to other types of data fusion and provides a framework for the study of more comprehensive properties of the biological network and other forms of complex networks.

摘要

将高通量数据整合到生物网络的系统和动态组织研究中一直是一项具有挑战性的任务。在此,我们提出了一种简单的层次聚类算法,该算法在很大程度上有助于实现这一目标。我们的方法通过将高通量蛋白质-蛋白质相互作用数据与添加的亚细胞定位和表达谱数据相结合,有效地揭示了酵母蛋白质-蛋白质相互作用网络的模块结构,并区分了蛋白质复合物和功能模块。此外,我们利用检测到的模块为模块内未表征的成分提供可靠的功能背景。另一方面,各种蛋白质-蛋白质关联信息的整合使我们的方法对假阳性具有鲁棒性,特别是对于衍生的蛋白质复合物。更重要的是,这种简单的方法可以自然地扩展到其他类型的数据融合,并为研究生物网络和其他形式的复杂网络的更全面特性提供一个框架。

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