Table 1 Metrics for identifying different types of mosaic variants from whole exome sequencing data. Values are based on ultra-high-depth sequencing validation results, and any uninformative results were excluded

From: Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing data

Type of mosaicism

Variant caller

Mosaic prioritisation

Validated mosaic

Validated constitutive or FP

Sensitivity

Specificity

PPV

NPV

De novo (child-PZM)

DNG

Binomial p < 0.0001

56

17

69%

84%

73%

80%

Binomial p ≥ 0.0001

24

81

VAF < 0.27

63

32

78%

68%

64%

84%

VAF ≥ 0.27

17

66

Inherited (low-level parent-PZM)

DNG

<2 alt reads in one parent

3

57

63%

89%

42%

95%

≥2 alt reads in one parent

5

7

Inherited (high-level parent-PZM)

GATK

Binomial p < 0.0001

9

7

69%

67%

56%

78%

Binomial p ≥ 0.0001

4

14

VAF < 0.27

13

12

100%

43%

52%

100%

VAF ≥ 0.27

0

9

  1. PZM postzygotic mosaicism, DNG DeNovoGear, GATK Genome Analysis Toolkit, VAF variant allele fraction from exome sequencing data, FP false positive, Binomial p = binomial test on the alternative allele reads, centred around 0.5, PPV positive predictive value, NPV negative predictive value