Table 2.
Method | Reference | |
---|---|---|
Perturb-seq | The Perturb-seq method combines a pooled CRISPR screen with single-cell RNA-seq by a guide barcode (GBC) expressed for each perturbation. | Prensner et al., 2021142 |
CRISP-seq: | The CRISP-seq technique allows the identification of the sgRNA that infects each individual cell by using a vector that contains the gRNA sequence and a transcribed polyadenylated unique guide index with a fluorescent selection marker. | Hanna and Doench, 2020141 |
Mosaic-seq: mosaic single-cell analysis by indexed CRISPR sequencing | Mosaic-seq couples CRISPRi with single-cell RNA sequencing. The library of vectors targeting enhancers also carries a unique barcode that allows the identification of the sgRNA. | Braun et al., 2016143 |
CROP-seq: CRISPR droplet sequencing | The CROP-seq method, unlike the other methods, does not pair the sgRNA with a barcode. Instead, the CROP-seq method uses the sgRNA as a barcode overlapping the Pol II transcript. | Manguso et al., 2017144 |
Summary of the different single-cell CRISPR methods currently available with a small description of the principle of the method.