Table 1 Single-cell sequencing reveals widespread on-target proximal deletions from CRISPR–Cas9

From: High-resolution genome-wide mapping of chromosome-arm-scale truncations induced by CRISPR–Cas9 editing

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%)

  1. 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.