Sun Rui, Cao Wenjie, Li ShengXuan, Jiang Jian, Shi Yazhou, Zhang Bengong
School of Mathematical & Physical Sciences, Wuhan Textile University, Wuhan, Hubei, China.
Center for Applied Mathematics and Interdisciplinary Studies, Wuhan Textile University, Wuhan, Hubei, China.
PLoS Comput Biol. 2024 Nov 25;20(11):e1012638. doi: 10.1371/journal.pcbi.1012638. eCollection 2024 Nov.
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.
细胞分化研究有助于更深入地理解生命的基本过程,阐明癌症等疾病的内在机制,并推动治疗学和精准医学的发展。现有的从单细胞RNA测序(scRNA-seq)数据推断细胞分化轨迹的方法主要依靠静态基因表达数据来测量细胞间的距离,进而推断伪时间轨迹。在这项工作中,我们引入了一种新方法scGRN-Entropy,用于从scRNA-seq数据推断细胞分化轨迹和伪时间。与现有方法不同,scGRN-Entropy通过纳入基因调控网络(GRN)中的动态变化来提高推断准确性。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,构建一个表示细胞间状态转换的无向图。然后,基于GRN空间中的细胞熵推断出的伪时间来细化无向图的边。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,通过与现有最先进方法的对比分析,证明了其在推断细胞分化轨迹方面的卓越性能。