Microfluidic single-cell multiomics analysis

被引:16
作者
Xu, Xing [1 ]
Zhang, Qiannan [1 ]
Li, Mingyin [1 ]
Lin, Shiyan [1 ]
Liang, Shanshan [1 ]
Cai, Linfeng [1 ]
Zhu, Huanghuang [1 ]
Su, Rui [1 ]
Yang, Chaoyong [1 ,2 ]
机构
[1] Xiamen Univ, Affiliated Hosp 1, Coll Chem & Chem Engn, Dept Chem Biol, Xiamen 361005, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, Inst Mol Med, Sch Med, Shanghai, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
cellular heterogeneity; microfluidics; multiomics analysis; single cell; GENOME-WIDE EXPRESSION; MESSENGER-RNA; HUMAN LUNG; SEQ; PROTEINS; ATLAS; TRANSCRIPTOMICS; QUANTIFICATION; HETEROGENEITY; CHROMATIN;
D O I
10.1002/VIW.20220034
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Cellular heterogeneity is essential to biological processes, such as embryonic development, cell differentiation, and the progression of disease. Recent years have seen the development of a variety of single-cell multiomics technologies that systemically codetect the genome, epigenome, transcriptome, and proteome for single-cell heterogeneity evaluation comprehensively. Microfluidics has emerged as a significant tool for single-cell multiomics techniques, enabling the analysis of the complex regulatory network associated with genome coding, epigenome regulation, and transcriptome/proteome expression in a single cell with increased detection sensitivity, accuracy, throughput, and integration. A review of state-of-the-art microfluidic single-cell multiomics analysis is presented here. Various microfluidics for isolating single cells are introduced first, highlighting their advantages, disadvantages, and applications in single-cell sequencing. Then, a comprehensive overview of microfluidic single-cell multiomics techniques is provided. In addition, a brief introduction of single-cell multiomics analysis in biological applications and clinical settings will be presented. Finally, we will conclude by discussing the future challenges and prospects of this field.
引用
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页数:28
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