表观基因组
计算生物学
单细胞测序
生物
疾病
DNA测序
转录组
生物信息学
基因
遗传学
DNA甲基化
外显子组测序
医学
突变
基因表达
病理
作者
Aimaiti Yasen,Abudusalamu Aini,Hui Wang,Wending Li,Chuanshan Zhang,Bo Ran,Tuerhongjiang Tuxun,Yusufukadier Maimaitinijiati,Yingmei Shao,Tuerganaili Aji,Hao Wen
标识
DOI:10.1016/j.meegid.2020.104198
摘要
Single-cell sequencing (SCS) is a next-generation sequencing method that is mainly used to analyze differences in genetic and protein information between cells, to obtain genetic information on microorganisms that are difficult to cultivate at a single-cell level and to better understand their specific roles in the microenvironment. By sequencing the whole genome, transcriptome and epigenome of a single cell, the complex heterogeneous mechanisms involved in disease occurrence and progression can be revealed, further improving disease diagnosis, prognosis prediction and monitoring of the therapeutic effects of drugs. In this study, we mainly summarized the methods and application fields of SCS, which may provide potential references for its future clinical applications, including the analysis of embryonic and organ development, the immune system, cancer progression, and parasitic and infectious diseases as well as stem cell research, antibody screening, and therapeutic research and development.
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