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firststeps [2009/03/05 14:20]
132.168.73.124
firststeps [2009/04/16 09:39] (current)
132.168.73.247
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 ====== Getting Started ====== ====== Getting Started ======
  
-This tutorial will show you how to validate a Mascot identification result with IRMa. A sample Mascot result file is available ​int the IRMa distribution (''<​IRMA_HOME>​/samples/​result_sample.dat''​). But the same operation could be executed with any Mascot MS/MS Ion Search result.+This tutorial will show you how to validate a Mascot identification result with IRMa. A sample Mascot result file is available ​in the [[ftp://ftp.cea.fr/​pub/​edyp/​irma|download section]] : ''​result_sample.dat''​. But the same operation could be executed with any Mascot MS/MS Ion Search result.  
 + 
 +**Note**: The ''​.dat''​ file should not be stored in a directory containing accent or blank.
  
 ===== Step 1 : Run IRMa ===== ===== Step 1 : Run IRMa =====
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 ===== Step 2 : Open and Parse a result file ===== ===== Step 2 : Open and Parse a result file =====
 +**Note**: The ''​.dat''​ file should not be stored in a directory containing accent or blank.
  
-Select Menu File --> Open --> Mascot Identification. In the //open dialog// go to the <​IRMa_HOME>/​samples directory and select result_sample.dat file. 
  
-In the first dialog, specify ​same parameters ​for Matrix Science parser ​(Almost, the same parameters as those proposed on mascot server ​search form are available here) :+Select Menu File --> Open --> Mascot Identification. ​In the //open dialog// select the ''​result_sample.dat''​ file. 
 + 
 +In this first dialog, ​you must specify ​the parameters ​that will be used to generate the result ​(almost, the same parameters as those proposed on mascot server ​result view):
   * Report Settings   * Report Settings
     * Report top (absolute or auto) : select Auto with p value < 0.05      * Report top (absolute or auto) : select Auto with p value < 0.05 
     * peptides cut-off : score = 20     * peptides cut-off : score = 20
-    * subsets ​threashold ​= 1, to consider all sub sets+    * subsets ​threshold ​= 1, to consider all sub sets
   * Parser Properties   * Parser Properties
     * Select "Never read sequence"​ (The result has been generated on our mascot server, so it sequence can't be retrieve in this case !)     * Select "Never read sequence"​ (The result has been generated on our mascot server, so it sequence can't be retrieve in this case !)
 +
 +{{ parser_settings.png?​300 | Parser settings}}
  
 ===== Step 3 : Filter results ===== ===== Step 3 : Filter results =====
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     * rank threshold = 1     * rank threshold = 1
  
 +{{ filter_settings.png?​300 | Filter settings}}
  
-===== Step 4 : Browse result ​=====+===== Step 4 : Result validation ​=====
  
 From Protein Centric Navigation Panel, you can select any identified protein hit to view its property (see User Guide Description...FIXME) From Protein Centric Navigation Panel, you can select any identified protein hit to view its property (see User Guide Description...FIXME)
- 
-===== Step 5 : Result curation ===== 
  
 They can be identified in the Protein Centric Navigation Panel, they are grayed ​ They can be identified in the Protein Centric Navigation Panel, they are grayed ​
 +
 +{{ hit_search.png?​500 | Hit search}}
  
 For example, ​ For example, ​
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   * In Protein Hit Tab, clik on first icon : <​IMG> ​   * In Protein Hit Tab, clik on first icon : <​IMG> ​
  
-It is also possible to delete all protein hits with no relevant peptides ​bu clicking on <​IMG_ALL_DEL>​ in general toolbox. +It is also possible to delete all protein hits with no relevant peptides ​by clicking on <​IMG_ALL_DEL>​ in general toolbox.
- +
-===== Step 6 : Export validated result ===== +
  
 +===== Step 5 : Export validated result =====
  
 +Once validated, the identification result can be exported into various formats. Click File -->​Export --> Identification result --> to Excel. Choose the name of the file that will be generated and click Save
firststeps.1236259200.txt.gz · Last modified: 2009/03/05 14:20 by 132.168.73.124