Ding Liang, Shi Hao, Qian Chenxi, Burdyshaw Chad, Veloso Joao Pedro, Khatamian Alireza, Pan Qingfei, Dhungana Yogesh, Xie Zhen, Risch Isabel, Yang Xu, Huang Xin, Yan Lei, Rusch Michael, Brewer Michael, Yan Koon-Kiu, Chi Hongbo, Yu Jiyang
Department of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Res Sq. 2023 Jan 27:rs.3.rs-2476875. doi: 10.21203/rs.3.rs-2476875/v1.
The sparse nature of single-cell omics data makes it challenging to dissect the wiring and rewiring of the transcriptional and signaling drivers that regulate cellular states. Many of the drivers, referred to as "hidden drivers", are difficult to identify via conventional expression analysis due to low expression and inconsistency between RNA and protein activity caused by post-translational and other modifications. To address this issue, we developed scMINER, a mutual information (MI)-based computational framework for unsupervised clustering analysis and cell-type specific inference of intracellular networks, hidden drivers and network rewiring from single-cell RNA-seq data. We designed scMINER to capture nonlinear cell-cell and gene-gene relationships and infer driver activities. Systematic benchmarking showed that scMINER outperforms popular single-cell clustering algorithms, especially in distinguishing similar cell types. With respect to network inference, scMINER does not rely on the binding motifs which are available for a limited set of transcription factors, therefore scMINER can provide quantitative activity assessment for more than 6,000 transcription and signaling drivers from a scRNA-seq experiment. As demonstrations, we used scMINER to expose hidden transcription and signaling drivers and dissect their regulon rewiring in immune cell heterogeneity, lineage differentiation, and tissue specification. Overall, activity-based scMINER is a widely applicable, highly accurate, reproducible and scalable method for inferring cellular transcriptional and signaling networks in each cell state from scRNA-seq data. The scMINER software is publicly accessible via: https://github.com/jyyulab/scMINER.
单细胞组学数据的稀疏性使得剖析调节细胞状态的转录和信号驱动因子的连接及重新连接具有挑战性。许多驱动因子,被称为“隐藏驱动因子”,由于表达水平低以及翻译后修饰和其他修饰导致的RNA与蛋白质活性不一致,难以通过传统的表达分析来识别。为了解决这个问题,我们开发了scMINER,这是一个基于互信息(MI)的计算框架,用于从单细胞RNA测序数据中进行无监督聚类分析以及细胞类型特异性推断细胞内网络、隐藏驱动因子和网络重新连接。我们设计scMINER以捕捉非线性的细胞-细胞和基因-基因关系并推断驱动因子活性。系统的基准测试表明,scMINER优于流行的单细胞聚类算法,尤其是在区分相似细胞类型方面。在网络推断方面,scMINER不依赖于仅适用于有限转录因子集的结合基序,因此scMINER可以为来自scRNA测序实验的6000多个转录和信号驱动因子提供定量活性评估。作为示例,我们使用scMINER揭示隐藏的转录和信号驱动因子,并剖析它们在免疫细胞异质性、谱系分化和组织特化中的调控子重新连接。总体而言,基于活性的scMINER是一种广泛适用、高度准确、可重复且可扩展的方法,用于从scRNA测序数据推断每个细胞状态下的细胞转录和信号网络。scMINER软件可通过以下链接公开获取:https://github.com/jyyulab/scMINER。