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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%