Hi Julian,

It depends on the file. Is it in centroid or profile mode? I'm not familiar 
with .d files so I don't know which it would be. If it is in profile mode you 
need to use the peak picking filter. Also, are you using the msconvertGUI.exe 
or running it through a shell like R?

Cheers,

Gavin.

________________________________
From: Julian Kang [manduma...@gmail.com]
Sent: 12 October 2011 22:04
To: mzmine-devel@lists.sourceforge.net
Subject: Re: [Mzmine-devel] Missing peaks in MzMine


Thanks for the quick response! I did open the mzXML file with the insilicos 
viewer, and saw that it must be a problem with the conversion from .d to 
.mzXML. Are there any alternatives to proteowizard that can do that or are 
there specific setting in proteowizard that I should be aware of to maximize 
conversion? Again thanks a bunch!


-Julian

Hi Julian,


Is that before or after processing with MzMine? You could try opening the mzXML 
file with the insilicos viewer 
(http://insilicos.com/products/insilicos-viewer-1) and compare that to the 
original .d file to check it is being converted properly.

Cheers,

Gavin.

From: Julian Kang [mailto:manduman88@<mailto:manduman88@>...]
Sent: 11 October 2011 19:25
To: mzmine-devel@...
Subject: [Mzmine-devel] Missing peaks in MzMine

Hi,

I converted an Agilent MS file (.d) to .mzXML using proteowizard so I can 
analyze the data using MzMine. However, when I compare some of the spectra from 
MzMine to Agilent Qualitative Analysis (4.0), I see that there are some very 
noticeable peaks in the Agilent Qual which are missing in MzMine. Is there any 
fix to this by chance? Thanks!

-Julian

--
Cornell University
Class of 2010
B.A. in Chemistry

--
Cornell University
Class of 2010
B.A. in Chemistry



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