计算机科学
推论
可扩展性
水准点(测量)
弹道
管道(软件)
数据挖掘
可用性
互补性(分子生物学)
集合(抽象数据类型)
机器学习
人工智能
生物
数据库
人机交互
物理
天文
程序设计语言
遗传学
地理
大地测量学
作者
Wouter Saelens,Robrecht Cannoodt,Helena Todorov,Yvan Saeys
标识
DOI:10.1038/s41587-019-0071-9
摘要
Trajectory inference approaches analyze genome-wide omics data from thousands of single cells and computationally infer the order of these cells along developmental trajectories. Although more than 70 trajectory inference tools have already been developed, it is challenging to compare their performance because the input they require and output models they produce vary substantially. Here, we benchmark 45 of these methods on 110 real and 229 synthetic datasets for cellular ordering, topology, scalability and usability. Our results highlight the complementarity of existing tools, and that the choice of method should depend mostly on the dataset dimensions and trajectory topology. Based on these results, we develop a set of guidelines to help users select the best method for their dataset. Our freely available data and evaluation pipeline ( https://benchmark.dynverse.org ) will aid in the development of improved tools designed to analyze increasingly large and complex single-cell datasets. The authors comprehensively benchmark the accuracy, scalability, stability and usability of 45 single-cell trajectory inference methods.
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