Center for Complex Network Research and Department of Physics, Northeastern University, Boston, Massachusetts, USA.
Nat Biotechnol. 2013 Aug;31(8):720-5. doi: 10.1038/nbt.2601. Epub 2013 Jul 14.
Predictions of physical and functional links between cellular components are often based on correlations between experimental measurements, such as gene expression. However, correlations are affected by both direct and indirect paths, confounding our ability to identify true pairwise interactions. Here we exploit the fundamental properties of dynamical correlations in networks to develop a method to silence indirect effects. The method receives as input the observed correlations between node pairs and uses a matrix transformation to turn the correlation matrix into a highly discriminative silenced matrix, which enhances only the terms associated with direct causal links. Against empirical data for Escherichia coli regulatory interactions, the method enhanced the discriminative power of the correlations by twofold, yielding >50% predictive improvement over traditional correlation measures and 6% over mutual information. Overall this silencing method will help translate the abundant correlation data into insights about a system's interactions, with applications ranging from link prediction to inferring the dynamical mechanisms governing biological networks.
对细胞成分之间的物理和功能联系的预测通常基于基因表达等实验测量之间的相关性。然而,相关性受到直接和间接路径的影响,这使得我们难以识别真正的成对相互作用。在这里,我们利用网络中动态相关性的基本特性来开发一种方法来消除间接效应。该方法接收节点对之间观察到的相关性作为输入,并使用矩阵变换将相关矩阵转换为高度可区分的静默矩阵,该矩阵仅增强与直接因果关系相关的项。针对大肠杆菌调控相互作用的经验数据,该方法将相关性的判别能力提高了两倍,与传统相关性度量相比,预测精度提高了 50%以上,与互信息相比,提高了 6%。总的来说,这种沉默方法将有助于将丰富的相关数据转化为对系统相互作用的深入了解,其应用范围从链路预测到推断控制生物网络的动态机制。