生物
计算生物学
转录组
胚胎干细胞
标识符
基因
RNA序列
遗传学
基因表达
计算机科学
程序设计语言
作者
Christoph Ziegenhain,Beate Vieth,Swati Parekh,Björn Reinius,Amy Guillaumet-Adkins,Martha Smets,Heinrich Leonhardt,Holger Heyn,Ines Hellmann,Wolfgang Enard
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2017-02-01
卷期号:65 (4): 631-643.e4
被引量:1380
标识
DOI:10.1016/j.molcel.2017.01.023
摘要
Single-cell RNA sequencing (scRNA-seq) offers new possibilities to address biological and medical questions. However, systematic comparisons of the performance of diverse scRNA-seq protocols are lacking. We generated data from 583 mouse embryonic stem cells to evaluate six prominent scRNA-seq methods: CEL-seq2, Drop-seq, MARS-seq, SCRB-seq, Smart-seq, and Smart-seq2. While Smart-seq2 detected the most genes per cell and across cells, CEL-seq2, Drop-seq, MARS-seq, and SCRB-seq quantified mRNA levels with less amplification noise due to the use of unique molecular identifiers (UMIs). Power simulations at different sequencing depths showed that Drop-seq is more cost-efficient for transcriptome quantification of large numbers of cells, while MARS-seq, SCRB-seq, and Smart-seq2 are more efficient when analyzing fewer cells. Our quantitative comparison offers the basis for an informed choice among six prominent scRNA-seq methods, and it provides a framework for benchmarking further improvements of scRNA-seq protocols.
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