生物
生物信息学
细胞
计算生物学
单细胞分析
核糖核酸
寡核苷酸
微流控
单细胞测序
标识符
基因组
DNA测序
细胞生物学
转录组
深度测序
基因
吞吐量
小RNA
遗传学
RNA序列
基因表达
表型
纳米技术
外显子组测序
计算机科学
材料科学
程序设计语言
无线
电信
作者
Tom Denyer,Marja C.P. Timmermans
标识
DOI:10.1016/j.tplants.2021.09.003
摘要
High-throughput, droplet-based single-cell RNA sequencing (scRNA-Seq) provides unprecedented resolution to examine cell–cell heterogeneity in tissues and organs. Microfluidic channels combine individual cells with uniquely barcoded beads to analyze transcriptomes of thousands of cells in parallel that can reconstruct the biological structure in silico. Individual cells can be traced back through bead/cell-specific barcodes on the oligos, and individual transcript amplification bias is accounted for with unique molecular identifiers (UMIs). scRNA-Seq has been used to identify unique cell types, states, and responses on a single-cell level. Combined with single nucleus-level assays of chromatin, scRNA-Seq provides further understanding of gene regulation networks.
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