Table 5 Probabilities for the event which each haploid at a particular locus is sequence at least twice
From: Genotyping of human neutrophil antigens (HNA) from whole genome sequencing data
Coverage | P(X1 > 1∩ X2 > 1) |
|---|---|
5 | 92.078% |
6 | 96.560% |
7 | 98.546% |
8 | 99.397% |
9 | 99.753% |
10 | 99.900% |
11 | 99.960% |
12 | 99.984% |
13 | 99.994% |
14 | 99.998% |
15 | 99.999% |