Integration of single-cell multi-omics for gene regulatory network inference

被引:37
作者
Hu, Xinlin [1 ]
Hu, Yaohua [1 ]
Wu, Fanjie [2 ]
Leung, Ricky Wai Tak [2 ]
Qin, Jing [2 ]
机构
[1] Shenzhen Univ, Coll Math & Stat, Shenzhen Key Lab Adv Machine Learning & Applicat, Shenzhen 518060, Peoples R China
[2] Sun Yat Sen Univ, Sch Pharmaceut Sci Shenzhen, Shenzhen 518107, Peoples R China
关键词
Single-cell sequencing; Gene regulatory network inference; Single-cell multi-omics integration; NONNEGATIVE MATRIX FACTORIZATION; DIFFERENTIAL-EQUATION MODELS; PARAMETER-ESTIMATION; EXPRESSION; REVEALS; SEQ; REGRESSION; OPTIMIZATION; SELECTION; SYSTEMS;
D O I
10.1016/j.csbj.2020.06.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2020 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
引用
收藏
页码:1925 / 1938
页数:14
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