I think the SeeMS tool from ProteoWizard may be your best bet. If you have
TPP installed, it may already be installed with TPP. Or otherwise, it is
easy to download and install. Install all of ProteoWizard, and then from
the Start menu under the ProteoWizard folder will be SeeMS.



Regards,

Eric





*From:* [email protected] <[email protected]>
*On Behalf Of *ilya gertsman
*Sent:* Friday, April 5, 2019 1:42 PM
*To:* [email protected]
*Subject:* Re: [spctools-discuss] Re: Combining the DIA Umpire results by
iProphet



Does anyone know of a good tool for viewing mzXML files, enabling one to
look at total ion current, perform XIC's for m/z's of interest, and other
basic functions (maybe something like AB Sciex's PeakView for .wiff files,
but only generic ms files formats)?  I saw a tool listed for TPP called
mzXML viewer, but do not see how to access this through TPP.  Any
recommendations would be greatly appreciated!

Many thanks!
ilya



On Fri, Apr 5, 2019 at 10:26 AM Ankit Balhara <[email protected]>
wrote:

Hi David,



Thanks for your kind help. Actually I am estimating the FDR by using the
Mayu tool, after combining the iprophet results of all the three datasets
which I have, as this gives me single Posterior probability (PPs/IPs) that
I am using in the SpectraST command line so as to generate the spectral
library.

Yes, I got the point which you have highlighted, but can I use Mayu for
estimating the FDR at final stage and then filter the results below the
threshold PP of FDR less than 1%, instead of filtering the results at each
iProphet analyses?



Thanks

Ankit









On Fri, 5 Apr 2019 at 20:03, David Shteynberg <
[email protected]> wrote:

Hello Ankit,



If you computer has the resources to handle all files then running one
iProphet job to combine the results will give you one analysis result with
FDR rates that apply to all the data.  If you do multiple iProphet runs
then you have to be more careful about how you combine the results because
your runs will overlap more in the correct result than the incorrect
results so simply taking all results together above an FDR threshold will
inflate your final FDR.  One easy way to do this is to divide the FDR by
the number of iProphet runs being combined.  For example if you split the
results into two iProphet analyses and you want the combined FDR to be less
than 1% you would filter each iProphet analyses at 0.5% FDR and then take
the total set.  Does that make sense?



Cheers,

-David



On Thu, Apr 4, 2019 at 8:57 AM Ankit Balhara <[email protected]>
wrote:

Thanks Felipe.



I have posted this issue in the issues section of DIA-Umpire issue tracker.



Ankit







On Thu, 4 Apr 2019 at 19:21, Felipe da Veiga Leprevost <
[email protected]> wrote:

Hi Ankit;



Please feel free to submit your DIA-Umpire questions and issues to our
DIA-Umpire issue tracker: https://github.com/Nesvilab/DIA-Umpire



Regards

On Wednesday, April 3, 2019 at 7:05:59 AM UTC-4, Ankit Balhara wrote:

Hi All,



I am analyzing the SWATH-MS data using the DIA-Umpire. And I have 3 data
files of same sample which lead to generation of 9 .mgf output files from
DIA-Umpire, which were converted into 9 mzXML and then subjected to Comet
and X! Tandem search, and subsequently to peptide prophet and hence total
files generated during this process are 18 pep.xml files.

My ultimate aim to build the assay library. So, I am confused how to
combine the results of these 18 peptideprophet files.



Should I combine the Comet search results of each data file separately and
X! Tandem results separately and then combine these outputs again using
iProphet? This should result in generation of 3 iprophet result files
corresponding to each data file, which can again combined into one file by
iProphet in final step?



Or there is another way out of this problem?



Thanks



Ankit

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*Ilya Gertsman, PhD*

*Owner/manager*

*7917 Ostrow St.*

*San Diego, CA 92111*

*www.clarusanalytical.com <http://www.clarusanalytical.com/>*

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