Singapore Immunology Network (SIgN), A*STAR, 8A Biomedical Grove, Immunos Building, Level 4, Singapore 138648, Singapore.
Singapore Immunology Network (SIgN), A*STAR, 8A Biomedical Grove, Immunos Building, Level 4, Singapore 138648, Singapore.
Mol Aspects Med. 2018 Feb;59:95-113. doi: 10.1016/j.mam.2017.10.004. Epub 2017 Nov 26.
Advances in single-cell RNA-sequencing have helped reveal the previously underappreciated level of cellular heterogeneity present during cellular differentiation. A static snapshot of single-cell transcriptomes provides a good representation of the various stages of differentiation as differentiation is rarely synchronized between cells. Data from numerous single-cell analyses has suggested that cellular differentiation and development can be conceptualized as continuous processes. Consequently, computational algorithms have been developed to infer lineage relationships between cell types and construct developmental trajectories along which cells are re-ordered such that similarity between successive cell pairs is maximized. Here, we compare and contrast the existing computational methods, and illustrate how they may be applied to build mouse myeloid progenitor lineages from massively parallel RNA single-cell sequencing data.
单细胞 RNA 测序技术的进步有助于揭示细胞分化过程中细胞异质性的先前未被充分认识的水平。单细胞转录组的静态快照很好地代表了分化的各个阶段,因为细胞之间的分化很少同步。来自许多单细胞分析的数据表明,细胞分化和发育可以被概念化为连续的过程。因此,已经开发了计算算法来推断细胞类型之间的谱系关系,并构建细胞重新排序的发育轨迹,使得连续细胞对之间的相似性最大化。在这里,我们比较和对比了现有的计算方法,并说明了如何将它们应用于从大规模平行 RNA 单细胞测序数据中构建小鼠髓系祖细胞谱系。