Hello,
I can see in the documentation for --hard-call-threshold that by it uses a threshold of a distance of 0.1 from the nearest hardcall to determine whether to set a genotype to missing when converting to hardcalls.
If I understand your distance calculation correctly, it’s based on dose for BOTH alleles, so if there was a C/T SNP and someone had a dosage of C=1.15/T=0.85 the calculation would be 0.5*(abs(1.15 – 1) + abs(0.85 – 1)) = 0.5*0.3 = distance of 0.15. Is that correct?
And if I want to calculate what the distance would have been for certain people on certain SNPs, can I use data exported with --export A to do that? Eg. if the .raw file shows the dose for one allele is 1.40784, does that mean the dose for the other allele is 2 - 1.40784 = 0.59216, and I can then use those two dosages to calculate distance? Or are there ever circumstances where the two dosages may not sum to 2 so I can’t infer what the other dosage was from the dosage shown in the .raw file?
Thank you,
Kristen
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