Table 1 |.
Technique | Single-cell isolation method | Reverse transcription method | cDNA amplification method |
Throughput (number of cells analysed) | UMI | Refs |
---|---|---|---|---|---|---|
Tang et al. | Micropipetting | Poly(A)-based | PCR | 101 | No | 10 |
inDrop | Droplet-based microfluidics system | Poly(A)-based | IVT | 104 | Yes | 20 |
Drop-seq | Droplet-based microfluidics system | Poly(A)-based | PCR | 104 | Yes | 21 |
Seq-Well | Microwells | Template-switching | PCR | 104 | Yes | 22 |
CytoSeq | Microwells | Poly(A)-based | PCR | 105 | Yes | 23 |
Div-seq | FACS | Template-switching | PCR | 103 (nuclei) | No | 24 |
DroNc-seq | Droplet-based microfluidics system | Template-switching | PCR | 104 (nuclei) | Yes | 25 |
STRT | Micropipetting | Template-switching | PCR | 102 | No | 159 |
CEL-seq | Micropipetting | Poly(A)-based | IVT | 102 | No | 170 |
SUPeR-seq | Micropipetting | Random primer-based | PCR | 102 | No | 171 |
Quartz-seq | FACS | Poly(A)-based | PCR | 102 | No | 172 |
MATQ-seq | Micropipetting | MALBAC primer-based | PCR | 102 | Yes | 162 |
SMART-seq2 | Micropipetting | Template-switching | PCR | 102 | No | 173 |
MARS-seq | FACS | Poly(A)-based | IVT | 103 | Yes | 161 |
CEL-seq2 | Microfluidic devices | Poly(A)-based | IVT | 102 | Yes | 160 |
Quartz-seq2 | FACS | Poly(A)-based | PCR | 103 | Yes | 174 |
SMART-seq | Micropipetting | Template-switching | PCR | 102 | No | 175 |
SC3-seq | Micropipetting | Poly(A)-based | PCR | 102 | Yes | 176 |
CEL-seq, cell expression by linear amplification and sequencing; CytoSeq, gene expression cytometry; Div-seq, RNA sequencing on divided cells; DroNc-seq, massively parallel single-nucleus sequencing with droplet technology; Drop-seq, droplet sequencing; FACS, fluorescence-activated cell sorting; IVT, in vitro transcription; MALBAC, multiple annealing and looping-based amplification cycles; MARS-seq, massively parallel single-cell RNA sequencing; MATQ-seq, multiple annealing and dC-tailing-based quantitative single-cell RNA sequencing; SC3-seq, single-cell mRNA 3′ end sequencing; seq2, second-generation platform; SMART-seq, switch mechanism at the 5′ end of RNA templates sequencing; STRT, single-cell tagged reverse transcription; SUPeR-seq, single-cell universal poly(A)-independent RNA sequencing; UMI, unique molecular identifier.