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
<p><b>Copyright information:</b></p><p>Taken from "Pedigree and genotype errors in the Framingham Heart Study"</p><p>http://www.biomedcentral.com/1471-2156/4/s1/S41</p><p>BMC Genetics 2003;4(Suppl 1):S41-S41.</p><p>Published online 31 Dec 2003</p><p>PMCID:PMC1866477.</p><p></p> We chose to blank genotypes with mistyping probabilities greater or equal to 0.25
