Li Lin, Xia Rui, Chen Wei, Zhao Qi, Tao Peng, Chen Luonan
Key Laboratory of Systems Biology, Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Brief Bioinform. 2023 Sep 20;24(5). doi: 10.1093/bib/bbad281.
Gene regulatory networks (GRNs) reveal the complex molecular interactions that govern cell state. However, it is challenging for identifying causal relations among genes due to noisy data and molecular nonlinearity. Here, we propose a novel causal criterion, neighbor cross-mapping entropy (NME), for inferring GRNs from both steady data and time-series data. NME is designed to quantify 'continuous causality' or functional dependency from one variable to another based on their function continuity with varying neighbor sizes. NME shows superior performance on benchmark datasets, comparing with existing methods. By applying to scRNA-seq datasets, NME not only reliably inferred GRNs for cell types but also identified cell states. Based on the inferred GRNs and further their activity matrices, NME showed better performance in single-cell clustering and downstream analyses. In summary, based on continuous causality, NME provides a powerful tool in inferring causal regulations of GRNs between genes from scRNA-seq data, which is further exploited to identify novel cell types/states and predict cell type-specific network modules.
基因调控网络(GRNs)揭示了控制细胞状态的复杂分子相互作用。然而,由于数据噪声和分子非线性,识别基因之间的因果关系具有挑战性。在此,我们提出了一种新的因果准则,即邻居交叉映射熵(NME),用于从稳态数据和时间序列数据推断基因调控网络。NME旨在基于变量与不同邻居大小的函数连续性,量化从一个变量到另一个变量的“连续因果关系”或功能依赖性。与现有方法相比,NME在基准数据集上表现出卓越的性能。通过应用于单细胞RNA测序(scRNA-seq)数据集,NME不仅可靠地推断了细胞类型的基因调控网络,还识别了细胞状态。基于推断出的基因调控网络及其进一步的活性矩阵,NME在单细胞聚类和下游分析中表现出更好的性能。总之,基于连续因果关系,NME为从scRNA-seq数据推断基因之间的基因调控网络因果调控提供了一个强大的工具,该工具可进一步用于识别新型细胞类型/状态并预测细胞类型特异性网络模块。