| Literature DB >> 31958516 |
Aimaiti Yasen1, Abudusalamu Aini2, Hui Wang3, Wending Li4, Chuanshan Zhang3, Bo Ran5, Tuerhongjiang Tuxun5, Yusufukadier Maimaitinijiati2, Yingmei Shao5, Tuerganaili Aji6, Hao Wen7.
Abstract
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.Entities:
Keywords: Application; Epigenetic sequencing; Single-cell sequencing; Whole-genome sequencing; Whole-transcriptome sequencing
Mesh:
Year: 2020 PMID: 31958516 DOI: 10.1016/j.meegid.2020.104198
Source DB: PubMed Journal: Infect Genet Evol ISSN: 1567-1348 Impact factor: 3.342