Dermadi Denis, Bscheider Michael, Bjegovic Kristina, Lazarus Nicole H, Szade Agata, Hadeiba Husein, Butcher Eugene C
Laboratory of Immunology and Vascular Biology, Department of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA; The Center for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System and the Palo Alto Veterans Institute for Research (PAVIR), Palo Alto, CA 94304, USA.
Laboratory of Immunology and Vascular Biology, Department of Pathology, School of Medicine, Stanford University, Stanford, CA 94305, USA; The Center for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System and the Palo Alto Veterans Institute for Research (PAVIR), Palo Alto, CA 94304, USA.
iScience. 2020 Feb 21;23(2):100842. doi: 10.1016/j.isci.2020.100842. Epub 2020 Jan 16.
High-dimensional single cell profiling coupled with computational modeling is emerging as a powerful tool to elucidate developmental programs directing cell lineages. We introduce tSpace, an algorithm based on the concept of "trajectory space", in which cells are defined by their distance along nearest neighbor pathways to every other cell in a population. Graphical mapping of cells in trajectory space allows unsupervised reconstruction and exploration of complex developmental sequences. Applied to flow and mass cytometry data, the method faithfully reconstructs thymic T cell development and reveals development and trafficking regulation of tonsillar B cells. Applied to the single cell transcriptome of mouse intestine and C. elegans, the method recapitulates development from intestinal stem cells to specialized epithelial phenotypes more faithfully than existing algorithms and orders C. elegans cells concordantly to the associated embryonic time. tSpace profiling of complex populations is well suited for hypothesis generation in developing cell systems.
高维单细胞分析与计算建模相结合,正成为阐明指导细胞谱系的发育程序的强大工具。我们引入了tSpace,这是一种基于“轨迹空间”概念的算法,其中细胞由它们沿着最近邻路径到群体中其他每个细胞的距离来定义。细胞在轨迹空间中的图形映射允许对复杂的发育序列进行无监督的重建和探索。应用于流式细胞术和质谱细胞术数据,该方法忠实地重建了胸腺T细胞发育,并揭示了扁桃体B细胞的发育和迁移调控。应用于小鼠肠道和秀丽隐杆线虫的单细胞转录组,该方法比现有算法更忠实地概括了从肠道干细胞到特化上皮表型的发育过程,并将秀丽隐杆线虫细胞与相关胚胎时间一致排序。复杂群体的tSpace分析非常适合在发育中的细胞系统中生成假设。