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. 2024 May 29;56(7):1482–1493. doi: 10.1038/s41588-024-01758-y

Table 1.

Single-cell sequencing reveals widespread on-target proximal deletions from CRISPR–Cas9

Perturbation type Dataset Cell type Total number of tested targets Tested loss direction Number of targets with specific loss Number of targets with loss toward telomere Number of targets with loss toward centromere
CRISPR–Cas9 Papalexi THP-1 (monocytic leukemia) 24 3′ 6 (25.0%) 5 (20.8%) 1 (4.2%)
5′ 1 (4.2%) 1 (4.2%) 0 (0.0%)
Frangieh Melanocytes (melanoma) 237 3′ 31 (13.1%) 23 (9.7%) 8 (3.4%)
5′ 34 (14.3%) 20 (8.4%) 14 (5.9%)
CRISPRi Replogle RPE1 2,066 3′ 45 (2.2%) 31 (1.5%) 14 (0.7%)
5′ 45 (2.2%) 11 (0.5%) 34 (1.6%)
Tian Induced pluripotent stem cell-derived neurons 177 3′ 3 (1.7%) 3 (1.7%) 0 (0.0%)
5′ 4 (2.3%) 2 (1.1%) 2 (1.1%)
Adamson K562 (leukemia) 78 3′ 1 (1.3%) 1 (1.3%) 0 (0.0%)
5′ 2 (2.6%) 1 (1.3%) 1 (1.3%)

The number and percent of target genes showing deletions specific to the target region in two CRISPR–Cas9 and three CRISPRi datasets uniformly reprocessed in scPerturb.