Department of Applied Mathematics, Computer Science and Statistics, Ghent University, Ghent 9000, Belgium.
Data Mining and Modeling for Biomedicine, VIB Center for Inflammation Research, Ghent 9052, Belgium.
Bioinformatics. 2020 Jul 1;36(Suppl_1):i66-i74. doi: 10.1093/bioinformatics/btaa463.
During the last decade, trajectory inference (TI) methods have emerged as a novel framework to model cell developmental dynamics, most notably in the area of single-cell transcriptomics. At present, more than 70 TI methods have been published, and recent benchmarks showed that even state-of-the-art methods only perform well for certain trajectory types but not others.
In this work, we present TinGa, a new TI model that is fast and flexible, and that is based on Growing Neural Graphs. We performed an extensive comparison of TinGa to five state-of-the-art methods for TI on a set of 250 datasets, including both synthetic as well as real datasets. Overall, TinGa improves the state-of-the-art by producing accurate models (comparable to or an improvement on the state-of-the-art) on the whole spectrum of data complexity, from the simplest linear datasets to the most complex disconnected graphs. In addition, TinGa obtained the fastest execution times, showing that our method is thus one of the most versatile methods up to date.
R scripts for running TinGa, comparing it to top existing methods and generating the figures of this article are available at https://github.com/Helena-todd/TinGa.
在过去的十年中,轨迹推断(TI)方法已经成为一种新的框架,可以对细胞发育动力学进行建模,尤其是在单细胞转录组学领域。目前,已经发表了超过 70 种 TI 方法,最近的基准测试表明,即使是最先进的方法,也只能很好地处理某些类型的轨迹,而不能处理其他类型的轨迹。
在这项工作中,我们提出了 TinGa,这是一种新的 TI 模型,它快速且灵活,基于生长神经网络图。我们在一组 250 个数据集上对 TinGa 与五种最先进的 TI 方法进行了广泛的比较,这些数据集包括合成数据集和真实数据集。总体而言,TinGa 通过在从最简单的线性数据集到最复杂的不连通图的整个数据复杂性范围内生成准确的模型(与最先进的方法相当或优于最先进的方法),提高了最先进的方法的性能。此外,TinGa 获得了最快的执行时间,这表明我们的方法是迄今为止最通用的方法之一。
用于运行 TinGa、将其与现有顶级方法进行比较以及生成本文图的 R 脚本可在 https://github.com/Helena-todd/TinGa 上获得。