scGRN-Entropy:利用单细胞数据和基于基因调控网络的转移熵推断细胞分化轨迹

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Rui Sun, Wenjie Cao, ShengXuan Li, Jian Jiang, Yazhou Shi, Bengong Zhang
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引用次数: 0

摘要

对细胞分化的研究有助于加深对生命基本过程的理解,阐明癌症等疾病的内在机制,推动治疗方法和精准医疗的发展。从单细胞 RNA 测序(scRNA-seq)数据推断细胞分化轨迹的现有方法主要依赖静态基因表达数据来测量细胞间的距离,然后推断伪时间轨迹。在这项工作中,我们介绍了一种从 scRNA-seq 数据中推断细胞分化轨迹和伪时间的新方法--scGRN-Entropy。与现有方法不同,scGRN-Entropy 结合了基因调控网络(GRN)的动态变化,从而提高了推断的准确性。在 scGRN-Entropy 中,通过整合基因表达空间中的静态关系和 GRN 空间中的动态关系,构建了代表细胞间状态转换的无向图。然后,根据 GRN 空间中的细胞熵推断出的伪时间对无向图的边进行细化。最后,应用最小生成树(MST)算法得出细胞分化轨迹。我们在八个不同的真实 scRNA-seq 数据集上验证了 scGRN-Entropy 的准确性,并通过与现有先进方法的比较分析,证明了它在推断细胞分化轨迹方面的卓越性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
scGRN-Entropy: Inferring cell differentiation trajectories using single-cell data and gene regulation network-based transfer entropy.

Research on cell differentiation facilitates a deeper understanding of the fundamental processes of life, elucidates the intrinsic mechanisms underlying diseases such as cancer, and advances the development of therapeutics and precision medicine. Existing methods for inferring cell differentiation trajectories from single-cell RNA sequencing (scRNA-seq) data primarily rely on static gene expression data to measure distances between cells and subsequently infer pseudotime trajectories. In this work, we introduce a novel method, scGRN-Entropy, for inferring cell differentiation trajectories and pseudotime from scRNA-seq data. Unlike existing approaches, scGRN-Entropy improves inference accuracy by incorporating dynamic changes in gene regulatory networks (GRN). In scGRN-Entropy, an undirected graph representing state transitions between cells is constructed by integrating both static relationships in gene expression space and dynamic relationships in the GRN space. The edges of the undirected graph are then refined using pseudotime inferred based on cell entropy in the GRN space. Finally, the Minimum Spanning Tree (MST) algorithm is applied to derive the cell differentiation trajectory. We validate the accuracy of scGRN-Entropy on eight different real scRNA-seq datasets, demonstrating its superior performance in inferring cell differentiation trajectories through comparative analysis with existing state-of-the-art methods.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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