In addition to Gavin's comments, I can answer for mzML and msconvert 
specifically. MzML has two
places to put "precursor m/z", either the "isolation target m/z" in the 
isolationWindow element or
the "selected ion m/z" in a selectedIon element.

On the Thermo Orbi or FT, the trigger mass is usually from the less accurate FT 
preview scan, so
that's what usually goes in the isolation target m/z. Later the full accuracy 
scan is done and
replaces the monoisotopic m/z in the scan trailer data. That's the value that 
msconvert puts in the
selected ion m/z.

For every other instrument, both values are going to be the same and what said 
Gavin applies (i.e.
it depends on the instrument whether it's monoisotopic or not).

-Matt


On 9/5/2011 3:07 AM, Gavin Blackburn wrote:
Hi RawProt,

Mono-isotopic is really dependant on the instrument rather than the file type. 
Instruments which
provide a more accurate mass will give you a more reliable mono-isotopic mass.

For example, on a quadrupole instrument hydorxy-l-proline and leucine will 
probably give the same
mass (132.1 m/z) for the H+ ion so this is not monoisotopic, whereas an 
Orbitrap will give you a
more accurate mass and hence a monoisotopic mass.

Of course, when the instrument is combined with some chromatography it is 
easier to identify
analytes based on both their mass and retention time, but to provide a true 
mono-isotopic mass
you need a capable instrument.

As far as I'm aware, converting from proprietary file format (.RAW, .WIFF etc.) 
to mzML or mzXML
retains all of the information contained within the original file but sets it 
out in a standard
format. Others on here will be able to give a better answer.


Cheers,

Gavin.

-----Original Message----- From: [email protected]
[mailto:[email protected]] On Behalf Of RawProt Sent: 03 
September 2011 21:29 To:
spctools-discuss Subject: [spctools-discuss] Does mzML(converted from RAW), 
WIFF, MGF, DTA, and
pepXML contains "mono-isotopic mass weight Information"?

Hi Experts,

I am somehow lost in the beginning phase of my first project in the Proteomics 
department. My
main task: "Designing DATABASE" of 
various "FILE" formats existed in the 
Proteomics research
(RAW, wiff, MGF, pepXML, dta). Till now main file 
formats are RAW, WIFF, MGF&  
DTA which are not
in XML and XML based: pepXM. 
Obviously there is overlap in information in 
multiple different
data 
file formats/experimental. Though analysis can be made from single file 
(experimental
measurements) or by comparison between “sets of files”. But, what is missing? 
Understanding the
re-occurring pattern in and between experiments.

Of course “Database” is needed in querying experiments/(files) with varied 
parameters. That’s why
file based searching is not efficient to our answer our question. What kind of 
"search term" in
an experiments? "Mono-isotopic mass".

"Have we seen this mono isotopic mass before in other experiments is the main 
issue in our
research"? I have started to work with RAW-> mzML (convert). I went through the 
documentation of
mzML available in the HUPO 
trying to design relational schema from mzML schema 
manually. Though
mzML is quite well documented I have confess not being clear.

Questions

--------------

1) Where information like*"mono isotopic mass"* are 
recorded in the mzML file? 
Is it precursor
charge attribute in the 
spectrum Element? Or am I missing something?

2) Can I be sure that all RAW and mzML after conversion regardless of different 
vendors consists
of "mono-isotopic mass" info?

3) Further, I am wondering does all mentioned files (wiff, pepXML,dta,mgf) 
too 
contains
"mono-isotopic mass" information?

4) If all files doesn't contain "mono-isotopic mass" info, then what are the 
most distinct term?

Please guide me!

Regards,


RawProt


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