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. Author manuscript; available in PMC: 2020 Oct 1.
Published in final edited form as: Nat Rev Cardiol. 2020 Mar 30;17(8):457–473. doi: 10.1038/s41569-020-0359-y

Table 1 |.

Most common scRNA-seq techniques

Technique UMI length (bp) Number of genes or cells analysed Sensitivity Dropout Amplification noise Cost per cell Single-cell capture method Year Refs
Full-length transcript
Smart-seq/C1 0 ++ ++ ++ ++++ +++ Plate 2012 22
Smart-seq2 0 +++ ++++ + +++ +++ Plate 2014 23
3ʹ-end counting
MARS-seq 8 + + +++ ++ +++ Microfluidic 2014 139
Drop-seq 8 + +++ +++ + ++ Droplet 2015 20
CEL-seq2/C1 6 +++ ++ ++ + +++ Microfluidic 2016 27
SORT-seq 4 +++ +++ ++ ++ ++ Plate 2016 71
10× Genomics 10 +++ ++ +++ + + Droplet 2017 28
mcSCRB-seq 10 ++ ++ ++ + +++ Plate 2018 140
5ʹ-end counting
WaferGen 10 +++ ++ ++ +++ +++ Nanowell 2017 141

CEL-seq, cell expression by linear amplification and sequencing; MARS-seq, massively parallel single-cell RNA-sequencing; mcSCRB-seq, molecular crowding single-cell RNA barcoding and sequencing; scRNA-seq, single-cell RNA sequencing; Smart-seq, switching mechanism at the 5′ end of the RNA template sequencing; SORT-seq, sorting and robot-assisted transcriptome sequencing; UMI, unique molecular identifier.