Entering edit mode
4.1 years ago
selplat21
▴
20
Hi all,
Does anyone have experience using BEAGLE on low coverage samples. I have about 500 individuals with ~3x genome-wide coverage and am trying to figure out the best arguments to use in BEAGLE to impute missing data.
Thank you.
Are these human samples? If not do you have a custom reference panel for your organism?