Gene regulatory network reconstruction: harnessing the power of single-cell multi-omic data

被引:36
作者
Kim, Daniel [1 ,2 ,3 ]
Tran, Andy [1 ,3 ,4 ]
Kim, Hani Jieun [2 ,3 ]
Lin, Yingxin [1 ,3 ,4 ]
Yang, Jean Yee Hwa [1 ,3 ,4 ]
Yang, Pengyi [1 ,2 ,3 ,4 ]
机构
[1] Univ Sydney, Sch Math & Stat, Camperdown, NSW, Australia
[2] Univ Sydney, Childrens Med Res Inst, Computat Syst Biol Unit, Camperdown, NSW, Australia
[3] Univ Sydney, Sydney Precis Data Sci Ctr, Camperdown, NSW, Australia
[4] Univ Sydney, Charles Perkins Ctr, Camperdown, NSW, Australia
基金
英国医学研究理事会;
关键词
TRANSCRIPTION FACTORS; PAIRED EXPRESSION; CAUSAL INFERENCE; CHIP-SEQ; CHROMATIN; ASSOCIATION; STATISTICS; BINDING; RNA;
D O I
10.1038/s41540-023-00312-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Inferring gene regulatory networks (GRNs) is a fundamental challenge in biology that aims to unravel the complex relationships between genes and their regulators. Deciphering these networks plays a critical role in understanding the underlying regulatory crosstalk that drives many cellular processes and diseases. Recent advances in sequencing technology have led to the development of state-of-the-art GRN inference methods that exploit matched single-cell multi-omic data. By employing diverse mathematical and statistical methodologies, these methods aim to reconstruct more comprehensive and precise gene regulatory networks. In this review, we give a brief overview on the statistical and methodological foundations commonly used in GRN inference methods. We then compare and contrast the latest state-of-the-art GRN inference methods for single-cell matched multi-omics data, and discuss their assumptions, limitations and opportunities. Finally, we discuss the challenges and future directions that hold promise for further advancements in this rapidly developing field.
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页数:13
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