Hi all!
I read your paper in Nature Biotechnology recently and I am interested in trying out your algorithm.
Does HLAthena have a feature to use an entire ORF or a protein as an input, and to predict good HLA binding peptides from those larger sequences?
It seems it can only predict already given peptides (or I am missing something?). I know that I could "chop" my protein into overlapping peptides using some other tool and use that list of peptides to run a batch screen on HLAthena, but was wondering if HLAthena has it already automated?
Thanks!
Stefan