Tornow Sabine, Mewes H W
Institute for Bioinformatics, German National Center for Health and Environment, Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany.
Nucleic Acids Res. 2003 Nov 1;31(21):6283-9. doi: 10.1093/nar/gkg838.
Genes and proteins are organized on the basis of their particular mutual relations or according to their interactions in cellular and genetic networks. These include metabolic or signaling pathways and protein interaction, regulatory or co-expression networks. Integrating the information from the different types of networks may lead to the notion of a functional network and functional modules. To find these modules, we propose a new technique which is based on collective, multi-body correlations in a genetic network. We calculated the correlation strength of a group of genes (e.g. in the co-expression network) which were identified as members of a module in a different network (e.g. in the protein interaction network) and estimated the probability that this correlation strength was found by chance. Groups of genes with a significant correlation strength in different networks have a high probability that they perform the same function. Here, we propose evaluating the multi-body correlations by applying the superparamagnetic approach. We compare our method to the presently applied mean Pearson correlations and show that our method is more sensitive in revealing functional relationships.
基因和蛋白质是根据它们特定的相互关系,或按照它们在细胞和遗传网络中的相互作用来组织的。这些网络包括代谢或信号通路、蛋白质相互作用、调控或共表达网络。整合来自不同类型网络的信息可能会引出功能网络和功能模块的概念。为了找到这些模块,我们提出了一种基于遗传网络中集体多体相关性的新技术。我们计算了一组基因(例如在共表达网络中)的相关强度,这些基因在另一个网络(例如在蛋白质相互作用网络中)中被确定为一个模块的成员,并估计了这种相关强度是偶然发现的概率。在不同网络中具有显著相关强度的基因组很有可能执行相同的功能。在此,我们提出通过应用超顺磁方法来评估多体相关性。我们将我们的方法与目前应用的平均皮尔逊相关性进行比较,并表明我们的方法在揭示功能关系方面更敏感。