4.8 Article

Comparative Analysis of Single-Cell RNA Sequencing Methods

Journal

MOLECULAR CELL
Volume 65, Issue 4, Pages 631-+

Publisher

CELL PRESS
DOI: 10.1016/j.molcel.2017.01.023

Keywords

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Funding

  1. Deutsche Forschungsgemeinschaft (DFG) through LMUexcellent
  2. Boehringer Ingelheim Fonds
  3. [SFB1243]
  4. [A01/A14/A15]

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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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