scShaper: an ensemble method for fast and accurate linear trajectory inference from single-cell RNA-seq data

被引:8
|
作者
Smolander, Johannes [1 ,2 ]
Junttila, Sini [1 ,2 ]
Venalainen, Mikko S. [1 ,2 ]
Elo, Laura L. [1 ,2 ,3 ]
机构
[1] Univ Turku, Turku Biosci Ctr, Tykistokatu 6, Turku 20520, Finland
[2] Abo Akad Univ, Tykistokatu 6, Turku 20520, Finland
[3] Univ Turku, Inst Biomed, Turku 20520, Finland
基金
芬兰科学院; 欧洲研究理事会;
关键词
D O I
10.1093/bioinformatics/btab831
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Computational models are needed to infer a representation of the cells, i.e. a trajectory, from single-cell RNA-sequencing data that model cell differentiation during a dynamic process. Although many trajectory inference methods exist, their performance varies greatly depending on the dataset and hence there is a need to establish more accurate, better generalizable methods. Results: We introduce scShaper, a new trajectory inference method that enables accurate linear trajectory inference. The ensemble approach of scShaper generates a continuous smooth pseudo-time based on a set of discrete pseudotimes. We demonstrate that scShaper is able to infer accurate trajectories for a variety of trigonometric trajectories, including many for which the commonly used principal curves method fails. A comprehensive benchmarking with state-of-the-art methods revealed that scShaper achieved superior accuracy of the cell ordering and, in particular, the differentially expressed genes. Moreover, scShaper is a fast method with few hyperparameters, making it a promising alternative to the principal curves method for linear pseudotemporal ordering.
引用
收藏
页码:1328 / 1335
页数:8
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