Closed barny116 closed 11 months ago
It is similar to the PD SN filter option. We remove PSMs with the intensity values falling in the lowest 5% (2.5% for PTM data). You can change these values, but what we set as defaults is what worked well for us in our tests.
Thank you so much for your prompt response. Also, is there anyway to add correction values for the individual TMT labels in MSFragger? Typically, I set the co-isolation threshold to 25% in PD. I believe that would be 75% in MSFragger's "min purity" option, as it is flipped? Is that correct? Thanks, Lea
On Wed, Mar 29, 2023 at 3:37 PM Alexey Nesvizhskii @.***> wrote:
It is similar to the PD SN filter option. We remove PSMs with the intensity values falling in the lowest 5% (2.5% for PTM data). You can change these values, but what we set as defaults is what worked well for us in our tests.
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We do not have the correction option. As far as Purity, yes it is flipped (so PD's 75% filter is Purity 25%. We recommend 50%, our default)
Awesome, thanks. Can you give me some insight on why your team chose not to include the correction step? -Lea
We extensively tested it as part of CPTAC consortium benchmarking, and it was not helping and even creating occasional problems. We disabled that option a while back. At any rate, we do not plan to add it back any time soon as we have other priorities.
Hi, I am new to using MSFragger, but I am really excited about its capabilities. I typically use PD to search my TMTPro 16-plex labeled peptide samples. However, I am trying a new application that PD is not suited for. Can you provide me with more information on the "min intensity (percent)" option? In my PD searches with TMT labels, I usually require a reporter ion S/N ratio of 10/1. Thanks, Lea