Oliver,

The Xpress chromatogram viewer lags Xpress in functionality and because of
this, can report a different ratio. There was functionality added to Xpress
which impacts the chromatogram reconstruction, such as the -p isotope
option, which never made it to the Xpress viewer.  So both tools can be
reconstructing the chromatograms using different settings, hence the
different numbers.  I believe that using "-p0" in the Xpress options will
cause the ratios calculated in Xpress and shown in the viewer to be the
same.  Otherwise there is no other solution/workaround until some work is
put in to resolve this discrepancy.  Maybe someday I'll feel guilty and
work on this when I have some free time but that hasn't been the case for
years now and this is simply a low priority issue for me personally.


On Thu, Mar 13, 2014 at 7:58 AM, [email protected]
<[email protected]>wrote:

> Dear all
>
> there is a discrepancy between Xpress values reported in interact.pep.xml
> and those Xpress values reported in the Xpress Viewer
> (XPressPeptideUpdateParser). For example, the Xpress column in
> interact.pep.xml reports a ratio of 1.40 while the Xpress viewer lists a
> ratio of 2.26. This is with TPP 4.7
>
> I think that this issue has been observed previously. Is there a
> solution/workaround for this?
>
> Thanks
>
> Oliver
>
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