no, have not tried Xpress. I preferred the way to visualize and analyze 
data on ASAP, and preferred it.... while it worked! thanks for the comment 
anyway

On Wednesday, 21 November 2012 12:45:01 UTC-4, kshitiz wrote:
>
> just curiois! have u tried XPRESS?? On large datasets, in our lab, ASAP 
> gave us a lot of problems while XPRESS worked. 
>
>
> On Wed, Nov 21, 2012 at 4:41 PM, Alex <[email protected] <javascript:>>wrote:
>
>> Thanks Brain for your quick reply,
>>
>> I'm running a dimethylation experiment (Ligth+28, Heavy+32). Until now, I 
>> have been acquiring data with a QTRAP2000, and everything worked nicely 
>> using the static approach (but not much proteome coverage with this MS). We 
>> now got a VelosPRO Orbitrap, and I am reacquiring the same samples!!!. I'm 
>> running X!Tandem, and DB search worked so far for protein ID. When I 
>> ANALYZE peptides with ASAPratio, things crash after 2-3 hours with this 
>> message. Until now, I have always been using the STATIC approach (according 
>> to the many threads I have reviewed on this topic), where I repeat the DB 
>> search for the light and heavy using two different parameters search. It 
>> used to work fine with the QTRAP2000 data. Of course, my files with the 
>> orbitrap are much larger, so I was suspecting I was running into some 
>> memory issue (Im not sure what this Runtime is all about).
>>
>> I'll try with your approach, if you have any other ideas, welcome!!!
>>
>> Alex
>>
>>
>> On Wednesday, 21 November 2012 10:40:06 UTC-4, Brian Hampton wrote:
>>
>>> I've never gotten the static option to work.  I'm not sure how the 
>>> static option is intended to be used..... correctly e.g. What type of data 
>>> set.
>>>
>>> If you are doing two searches one with the static light and the second 
>>> with the static heavy isotope labels, you will have to redo the search and 
>>> do it as per the Tandem API where you set the light to be a static mod and 
>>> the mass difference between the heavy and light to be a variable mod.  In 
>>> addition to giving results ASAPRatio can quantitate, it has been noted that 
>>> the second search method is more statistically sound because it increases 
>>> the size of the database as a result of the variable mods.
>>>
>>> Using the second search strategy has reduced ASAPRatio processing time 
>>> on my data sets from  many hours to about a half hour.  Also, using the 
>>> static option on Linux w/ TPP 4.5.2 ASAPRatio would complete after hours. 
>>>  But I have problems with the viewers not working in Linux so after 
>>> switching to Win for the quan analysis, using TPP 4.6.1 the static option 
>>> always kicks out an error and quits.  Feeding it search results as 
>>> mentioned above it all works and completes much more quickly.
>>>
>>> Why the static option doesn't work on our data sets is a mystery to me.
>>>
>>> Brian
>>>
>>>
>>> On Nov 21, 2012, at 8:33 AM, Alex <[email protected]> wrote:
>>>
>>> I think my post didn't show up correctly. Here it goes again!
>>>
>>> Hi TTP community,
>>>
>>> I'm running some ASAPratio quant on a 2D-LC-MSMS experiment on windows 
>>> XP running TPP v4.5 RAPTURE rev 2, Build 201202031108 (MinGW). After a
>>>  couple of hours analysis I get the following error. Has somebody run 
>>> into this problem before??? Any ideas much appreciated!!!
>>>
>>>
>>> Alex
>>>
>>>
>>> Error Message:
>>>
>>> This application has requested the Runtime to terminate it in an unusual 
>>> way.
>>> Please contact the application's support team for more information.
>>> command "C:/Inetpub/tpp-bin/**ASAPRatioPeptideParser "interact.pep.xml" 
>>> -lKn -F -C -r0.1 -S -mK160.15137n33.06425" failed: No such process
>>> command "C:/Inetpub/tpp-bin/**ASAPRatioPeptideParser "interact.pep.xml" 
>>> -lKn -F -C -r0.1 -S -mK160.15137n33.06425" exited with non-zero exit code: 3
>>> QUIT - the job is incomplete
>>> command "c:\Inetpub\tpp-bin\xinteract -Ninteract.pep.xml -p0.05 -l7 -Op 
>>> -I1 -I4 -I5 -A-lKn-F-C-r0.1-S-mK160.**15137n33.06425 
>>> 2DYeast01.tandem.pep.xml
>>> 2DYeast02.tandem.pep.xml 2DYeast03.tandem.pep.xml 
>>> 2DYeast04.tandem.pep.xml 2DYeast05.tandem.pep.xml 2DYeast06.tandem.pep.xml 
>>> 2DYeast07.tandem.pep.xml 2DYeast08.tandem.pep.xml 
>>> 2DYeast09.tandem.pep.xml 2DYeast10.tandem.pep.xml 2DYeast11.tandem.pep.xml 
>>> 2DYeast12.tandem.pep.xml 2DYeast13.tandem.pep.xml 
>>> 2DYeast14.tandem.pep.xml 2DYeast15.tandem.pep.xml 2DYeast16.tandem.pep.xml 
>>> 2DYeast17.tandem.pep.xml 2DYeast18.tandem.pep.xml 
>>> 2DYeast19.tandem.pep.xml 2DYeast20.tandem.pep.xml 2DYeast21.tandem.pep.xml 
>>> 2DYeast22.tandem.pep.xml 2DYeast23.tandem.pep.xml 
>>> H2DYeast01.tandem.pep.xml H2DYeast02.tandem.pep.xml 
>>> H2DYeast03.tandem.pep.xml 
>>> H2DYeast04.tandem.pep.xml H2DYeast05.tandem.pep.xml 
>>> H2DYeast06.tandem.pep.xml H2DYeast07.tandem.pep.xml 
>>> H2DYeast08.tandem.pep.xml 
>>> H2DYeast09.tandem.pep.xml H2DYeast10.tandem.pep.xml 
>>> H2DYeast11.tandem.pep.xml H2DYeast12.tandem.pep.xml 
>>> H2DYeast13.tandem.pep.xml 
>>> H2DYeast14.tandem.pep.xml H2DYeast15.tandem.pep.xml 
>>> H2DYeast16.tandem.pep.xml H2DYeast17.tandem.pep.xml 
>>> H2DYeast18.tandem.pep.xml 
>>> H2DYeast19.tandem.pep.xml H2DYeast20.tandem.pep.xml 
>>> H2DYeast21.tandem.pep.xml H2DYeast22.tandem.pep.xml 
>>> H2DYeast23.tandem.pep.xml" failed: No 
>>> such process
>>>
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>
>
> -- 
> Kshitiz Tyagi
>
>
>  

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