Is it possible for us to get the total number of reads at the variant position?
##INFO=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth; some reads may have been filtered">
This will help us in the allele fraction calculations.
Kindly revert back if possible guys.
thanks,
Venki
Venkatesh Chellappa
Is it possible for us to get the total number of reads at the variant position?
##INFO=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth; some reads may have been filtered">This will help us in the allele fraction calculations.
Kindly revert back if possible guys.
thanks,
Venki
Venkatesh Chellappa