Hello Rene
Thanks for using the tools and double checking your work.
In my tests I have found that applying the NSP model at the iProphet step greatly improves performance on peptide level. And applying the NSP model at the ProteinProphet step improves performance on the protein level. The two models are somewhat different since the ProteinProphet model considers grouping information while the iProphet model doesnt. I have not found the two to interfere.
A safe and conservative approach so would look at the conservative estimate e.g. ProteinProphet probability cutoff to give me 1% error with decoys or 1% error with the model which ever is more conservative.
When the model tends to underestimate error on protein or peptide level this is usually stemming from underestimation at the spectrum level by PeptideProphet and can be controlled by the CLEVEL={value} option for PeptideProphetParser -c{value} for xinteract. Setting this to a number greater than zero like .5 or 1 or 2 will serve to make the model more conservative overall, a negative value will have opposite effect which will carry through to the peptide and protein levels.
Also I am curious why you set decoy rate to 0.25?
Best,
David
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Maybe “decoy fraction” is the right term for this concept?
Sure, decoy rate sounds good, much better than the decoy ratio.
Thanks,
Eric