Hi Matt,

Thanks, this seems to have done the trick. I now have a 14 GB mzXML file
instead of 50 GB.

I am interested to know whether the peak picking is being done with
MassHunter or Proteowizard in this case?

Many thanks,
Ben.


On Thu, Sep 24, 2009 at 2:21 PM, Matt Chambers <
[email protected]> wrote:

>
> Hi Ben,
>
> 50gb for one file? That's impressive. That could be much improved with
> compression (which the Agilent MH format also does), but since you need
> to peak pick the MSn to identify them in most search engines, try this
> command:
> msconvert source.d --mzXML --filter "peakPicking true [2,2]"
> There is a bug in msconvert's Reader_Agilent (actually I think it's in
> MHDAC; I'm looking into it now with Agilent) that sometimes will always
> centroid profile data no matter whether it was requested or not. So even
> though the above command doesn't specify to peak pick the MS1s, it may
> do so anyway. If that's the case, let me know and I can get you a fixed
> build with a workaround in place.
>
> -Matt
>
>
> Ben Collins wrote:
> > Hi all,
> >
> > I have data from an Agilent QTOF (.d) collected in profile mode (both
> > MS1 and MS2) and I would like to convert to mzXML which I can do with
> > Trapper or msconvert. The question I have is, is it possible to
> > perform centroiding only on the MS2 data while leaving the MS1 data in
> > profile mode?
> >
> > Unfortunately it's not currently possible to collect MS1 in profile
> > and MS2 in centroid on this instrument (I have requrested it from the
> > vendor). The issue is that if both files are in profile mode the files
> > is pretty unmanageable (up to 50 GB) but I need to keep the MS1 data
> > in profile to do AMT/label free analysis.
> >
> > Thanks,
> > Ben
> >
>
>
> >
>

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