Figure 4
From: Pedigree and genotype errors in the Framingham Heart Study
Distribution of double-recombinant genotyping errors The distribution of mistyping probabilities for the markers in chromosome 7 is shown on the left, and the proportion of genotypes blanked on the right, as determined by the mistyping probability thresholds on the x-axis. We chose to blank genotypes with mistyping probabilities greater or equal to 0.25.