I'm just requesting the addition of the ability to compute the binding strength for the corresponding wild-type peptides for SNV-derived peptides.
As a stop-gap workaround, is it useful to just supply an altered variant file where the variant column is set to be the same as the wild-type, or to flip the two round so I can get Topiary to chuck out affinity estimates for those peptides?
Hi there ,
I'm just requesting the addition of the ability to compute the binding strength for the corresponding wild-type peptides for SNV-derived peptides.
As a stop-gap workaround, is it useful to just supply an altered variant file where the variant column is set to be the same as the wild-type, or to flip the two round so I can get Topiary to chuck out affinity estimates for those peptides?