I'm reading this MoFi paper right now, and it's reminding me of @veitveit's concern that we need to allow room for scores in PTMs.
I think we might need to formalize a solution for at least two categories of scores:
- likelihoods of localization
- likelihood of different modifications at the same position accounting for the same mass difference
- We have come upon this problem in Proteoform Suite, and they've come upon it in this paper.
- In the text they give the example (with glycans): "For instance, assume that a given residual mass may be compatible with the glycoforms A2G0F/A2G2F and A2G1F/A2G1F, whose scores are 0.7 and 0.3, respectively. Then, the former permutation will account for 70% of the peak abundance, while the latter one will explain the remaining 30%."
- How should we note this type of likelihood for two different modifications at the same position?
Can anyone think of more categories of scores?
I'm reading this MoFi paper right now, and it's reminding me of @veitveit's concern that we need to allow room for scores in PTMs.
I think we might need to formalize a solution for at least two categories of scores:
PROT[Phospho|#mod:20]EOFORMS[Phospho|#mod:80], as noted in Ambiguity of PTM localization #17Can anyone think of more categories of scores?