转录组
计算生物学
单细胞分析
生物
基因表达谱
小桶
细胞
人口
生物信息学
基因
基因表达
遗传学
医学
环境卫生
作者
Punit Bhattachan,Marc G. Jeschke
出处
期刊:Shock
[Ovid Technologies (Wolters Kluwer)]
日期:2023-11-10
标识
DOI:10.1097/shk.0000000000002274
摘要
The analysis of the single-cell transcriptome has emerged as a powerful tool to gain insights of the basic mechanisms of health and disease. It is widely used to reveal the cellular diversity and complexity of tissues at cellular resolution by RNA sequencing of the whole transcriptome from a single cell. Equally, it is applied to discover an unknown, rare population of cells in the tissue. The prime advantage of single-cell transcriptome analysis is the detection of stochastic nature of gene expression of the cell in tissue. Moreover, the availability of multiple platforms for the single-cell transcriptome has broadened its approaches to using cells of different sizes and shapes, including the capture of short or full-length transcripts, which is helpful in the analysis of challenging biological samples. And with the development of numerous packages in R and Python, new directions in the computational analysis of single-cell transcriptomes can be taken to characterize healthy versus diseased tissues to obtain novel pathological insights. To further examine the biology of different cell types, downstream analysis such as differential gene expression analysis, GO term analysis, KEGG pathway analysis, cell-cell interaction analysis, and trajectory analysis has become standard practice in the workflow of single-cell transcriptome analysis. Here, we provide a broad overview of single-cell transcriptome analysis in health and disease conditions currently applied in various studies.
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