TrAGEDy-trajectory alignment of gene expression dynamics.

Ross F Laidlaw, Emma M Briggs, Keith R Matthews, Amir Madany Mamlouk, Richard McCulloch, Thomas D Otto
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Abstract

Motivation: Single-cell transcriptomics sequencing is used to compare different biological processes. However, often, those processes are asymmetric which are difficult to integrate. Current approaches often rely on integrating samples from each condition before either cluster-based comparisons or analysis of an inferred shared trajectory.

Results: We present Trajectory Alignment of Gene Expression Dynamics (TrAGEDy), which allows the alignment of independent trajectories to avoid the need for error-prone integration steps. Across simulated datasets, TrAGEDy returns the correct underlying alignment of the datasets, outperforming current tools which fail to capture the complexity of asymmetric alignments. When applied to real datasets, TrAGEDy captures more biologically relevant genes and processes, which other differential expression methods fail to detect when looking at the developments of T cells and the bloodstream forms of Trypanosoma brucei when affected by genetic knockouts.

Availability and implementation: TrAGEDy is freely available at https://github.com/No2Ross/TrAGEDy, and implemented in R.

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TrAGEDy--基因表达动态的轨迹对齐。
动机:单细胞转录组测序用于比较不同的生物过程。然而,这些过程往往是不对称的,难以整合。目前的方法通常依赖于在基于聚类的比较或推断的共享轨迹分析之前,从每个条件中整合样本。结果:我们提出了基因表达动力学的轨迹对齐(悲剧),它允许独立的轨迹对齐,以避免需要容易出错的整合步骤。在模拟数据集中,TrAGEDy返回数据集的正确底层对齐,优于当前无法捕获非对称对齐复杂性的工具。当应用于真实的数据集时,TrAGEDy捕获了更多与生物学相关的基因和过程,这是其他差异表达方法在观察T细胞的发育和布鲁氏锥虫的血流形式受到基因敲除影响时无法检测到的。可用性和实施:TrAGEDy可在https://github.com/No2Ross/TrAGEDy免费获得,并在r中实现。补充信息:补充信息可在Bioinformatics在线获得。
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