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Currently, pVACseq does not prefilter transcripts on their biotype. We prioritize protein_coding transcripts when picking the best peptide and transcript in the aggregate report creation.
In pVACsplice we hard-pre-filter on protein_coding transcripts.
Instead we should define a new parameter --biotypes with a default of ['protein_coding'] that applies a prefilter on transcript biotypes both in pVACseq and pVACsplice. The aggregate report will continue to prioritize protein_coding transcripts when selecting the best peptide/transcripts. The docs should explain that "a few other, more speculative types (e.g. non_stop_decay and nonsense_mediated_decay) can give rise to neoantigens if users want to include them, they can specify their own list of biotypes".
The text was updated successfully, but these errors were encountered:
hi I'm wondering when pVACsplice will be ready for use? I read your publication regarding pVACsplice but now I'm confused when I see that there is no pVACsplice in the pVACtools suite.
Hi @sufyazi, we are currently doing extensive testing on this tool on various patient data and are hoping to release it before the end of the year. May I ask which publication you are referencing? While we've presented this tool at various conferences, we haven't published a full paper on it yet.
Hi Susanna, sorry if I was implying the wrong thing. I saw an abstract of pVacSplice here 10.1016/j.cancergen.2022.10.114 and wanted to find out more about it, only to realize it is not yet there in pVacTools. I just started using pVacTools at work for a new project we are embarking, and pVacSplice sounds perfect to incorporate into our pipeline, so I was just wondering.
Thank you for the update! I will look forward to it!
Currently, pVACseq does not prefilter transcripts on their biotype. We prioritize protein_coding transcripts when picking the best peptide and transcript in the aggregate report creation.
In pVACsplice we hard-pre-filter on protein_coding transcripts.
Instead we should define a new parameter
--biotypes
with a default of['protein_coding']
that applies a prefilter on transcript biotypes both in pVACseq and pVACsplice. The aggregate report will continue to prioritize protein_coding transcripts when selecting the best peptide/transcripts. The docs should explain that "a few other, more speculative types (e.g.non_stop_decay
andnonsense_mediated_decay
) can give rise to neoantigens if users want to include them, they can specify their own list of biotypes".The text was updated successfully, but these errors were encountered: