Luo Ruiyan, Zhao Hongyu
Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Ann Appl Stat. 2011;5(2A):725-745. doi: 10.1214/10-AOAS425.
Recent technological advances have made it possible to simultaneously measure multiple protein activities at the single cell level. With such data collected under different stimulatory or inhibitory conditions, it is possible to infer the causal relationships among proteins from single cell interventional data. In this article we propose a Bayesian hierarchical modeling framework to infer the signaling pathway based on the posterior distributions of parameters in the model. Under this framework, we consider network sparsity and model the existence of an association between two proteins both at the overall level across all experiments and at each individual experimental level. This allows us to infer the pairs of proteins that are associated with each other and their causal relationships. We also explicitly consider both intrinsic noise and measurement error. Markov chain Monte Carlo is implemented for statistical inference. We demonstrate that this hierarchical modeling can effectively pool information from different interventional experiments through simulation studies and real data analysis.
最近的技术进步使得在单细胞水平上同时测量多种蛋白质活性成为可能。利用在不同刺激或抑制条件下收集到的数据,就有可能从单细胞干预数据中推断蛋白质之间的因果关系。在本文中,我们提出了一个贝叶斯层次建模框架,用于基于模型中参数的后验分布来推断信号通路。在此框架下,我们考虑网络稀疏性,并对所有实验的总体水平以及每个单独实验水平上两种蛋白质之间关联的存在进行建模。这使我们能够推断相互关联的蛋白质对及其因果关系。我们还明确考虑了内在噪声和测量误差。通过马尔可夫链蒙特卡罗方法进行统计推断。我们通过模拟研究和实际数据分析证明,这种层次建模可以有效地整合来自不同干预实验的信息。