Hu Xinlin, Hu Yaohua, Wu Fanjie, Leung Ricky Wai Tak, Qin Jing
Shenzhen Key Laboratory of Advanced Machine Learning and Applications, College of Mathematics and Statistics, Shenzhen University, Shenzhen 518060, China.
School of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Shenzhen 518107, China.
Comput Struct Biotechnol J. 2020 Jun 29;18:1925-1938. doi: 10.1016/j.csbj.2020.06.033. eCollection 2020.
The advancement of single-cell sequencing technology in recent years has provided an opportunity to reconstruct gene regulatory networks (GRNs) with the data from thousands of single cells in one sample. This uncovers regulatory interactions in cells and speeds up the discoveries of regulatory mechanisms in diseases and biological processes. Therefore, more methods have been proposed to reconstruct GRNs using single-cell sequencing data. In this review, we introduce technologies for sequencing single-cell genome, transcriptome, and epigenome. At the same time, we present an overview of current GRN reconstruction strategies utilizing different single-cell sequencing data. Bioinformatics tools were grouped by their input data type and mathematical principles for reader's convenience, and the fundamental mathematics inherent in each group will be discussed. Furthermore, the adaptabilities and limitations of these different methods will also be summarized and compared, with the hope to facilitate researchers recognizing the most suitable tools for them.
近年来,单细胞测序技术的进步为利用一个样本中数千个单细胞的数据重建基因调控网络(GRN)提供了契机。这揭示了细胞中的调控相互作用,并加速了疾病和生物过程中调控机制的发现。因此,已经提出了更多利用单细胞测序数据重建GRN的方法。在本综述中,我们介绍了单细胞基因组、转录组和表观基因组的测序技术。同时,我们概述了利用不同单细胞测序数据的当前GRN重建策略。为方便读者,生物信息学工具按其输入数据类型和数学原理进行了分组,并将讨论每组中固有的基本数学原理。此外,还将总结和比较这些不同方法的适应性和局限性,希望有助于研究人员识别最适合他们的工具。