Mitra Riten, Müller Peter, Qiu Peng, Ji Yuan
Department of Bioinformatics and Biostatistics, University of Louisville, Louisville, KY, USA.
Department of Mathematics, The University of Texas at Austin, Austin, TX, USA.
Cancer Inform. 2014 Dec 10;13(Suppl 4):79-89. doi: 10.4137/CIN.S13984. eCollection 2014.
We propose a class of hierarchical models to investigate the protein functional network of cellular markers. We consider a novel data set from single-cell proteomics. The data are generated from single-cell mass cytometry experiments, in which protein expression is measured within an individual cell for multiple markers. Tens of thousands of cells are measured serving as biological replicates. Applying the Bayesian models, we report protein functional networks under different experimental conditions and the differences between the networks, ie, differential networks. We also present the differential network in a novel fashion that allows direct observation of the links between the experimental agent and its putative targeted proteins based on posterior inference. Our method serves as a powerful tool for studying molecular interactions at cellular level.
我们提出了一类层次模型来研究细胞标志物的蛋白质功能网络。我们考虑了一个来自单细胞蛋白质组学的新数据集。这些数据是通过单细胞质谱流式细胞术实验生成的,在该实验中,针对多个标志物在单个细胞内测量蛋白质表达。测量了数万个细胞作为生物学重复样本。应用贝叶斯模型,我们报告了不同实验条件下的蛋白质功能网络以及这些网络之间的差异,即差异网络。我们还以一种新颖的方式呈现差异网络,该方式基于后验推断允许直接观察实验试剂与其假定的靶向蛋白质之间的联系。我们的方法是研究细胞水平分子相互作用的有力工具。