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Time-resolved single-cell transcriptomic sequencing

delete2024-01-01
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OA
AI
X
Xing Xu
W
Wen, Qianxi
L
Lan, Tianchen
S
Shiyan Lin
Q
Qiu, Minghao
N
Na Xing
C
Chaoyong Yang *
DOI:10.1039/d4sc05700gdelete
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摘要

摘要

En 中文
Cells experience continuous transformation under both physiological and pathological circumstances. Single-cell RNA sequencing (scRNA-seq) is competent in disclosing the disparities of cells; nevertheless, it poses challenges in linking the individual cell state at distinct time points. Although computational approaches based on scRNA-seq data have been put forward for trajectory analysis, the result is based on assumptions and fails to reflect the actual states. Consequently, it is necessary to incorporate a time anchor into the scRNA-seq library for the temporal documentation of the dynamic expression pattern. This review comprehensively overviews the time-resolved single-cell transcriptomic sequencing methodologies and applications. As scRNA-seq functions as the basis for profiling single-cell expression patterns, the review initially introduces various scRNA-seq approaches. Subsequently, the review focuses on the different experimental strategies for introducing a time anchor to scRNA-seq, highlighting their principles, strengths, weaknesses, and comparing their adaptation in various scenarios. Next, it provides a brief summary of applications in immunity response, cancer progression, and embryo development. Finally, the review concludes with a forward-looking perspective on future advancements in time-resolved single-cell transcriptomic sequencing.
Keyword:
GENE-EXPRESSION
RNA-SEQ
DYNAMICS
TRAJECTORIES
CANCER
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期刊

Chemical Science 封面图
Chemical Science
IF:
7.4
论文数:
1.7W
被引数:
9.3W

机构

X
xiamen university
学者数:
5.9W
论文数: 3.8W
被引数: 67
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