单细胞测序
转录组
核糖核酸
单细胞分析
计算生物学
基因
细胞
基因表达
人口
生物
遗传学
外显子组测序
突变
社会学
人口学
作者
Yuguang Liu,Patricio Jeraldo,Jin Sung Jang,Bruce W. Eckloff,Jin Jen,Marina Walther-Antonio
标识
DOI:10.1021/acs.analchem.8b04773
摘要
Single cell RNA sequencing is a technology that provides the capability of analyzing the transcriptome of a single cell from a population. So far, single cell RNA sequencing has been focused mostly on human cells due to the larger starting amount of RNA template for subsequent amplification. One of the major challenges of applying single cell RNA sequencing to microbial cells is to amplify the femtograms of the RNA template to obtain sufficient material for downstream sequencing with minimal contamination. To achieve this goal, efforts have been focused on multiround RNA amplification, but would introduce additional contamination and bias. In this work, we for the first time coupled a microfluidic platform with multiple displacement amplification technology to perform single cell whole transcriptome amplification and sequencing of Porphyromonas somerae, a microbe of interest in endometrial cancer, as a proof-of-concept demonstration of using single cell RNA sequencing tool to unveil gene expression heterogeneity in single microbial cells. Our results show that the bacterial single-cell gene expression regulation is distinct across different cells, supporting widespread heterogeneity.
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