Frequently Asked Questions

Tutorial Questions

How many search engines can you use in SearchGUI?

Question: How many search engines can you use in SearchGUI?

SearchGUI has options to use upto 9 search algorithms. However, running all at the same time can be time consuming. According to our initial test, upto 4 search engines can give you good results.

In the MVP platform, is it possible to view the genomic location of all the peptides?

Question: In the MVP platform, is it possible to view the genomic location of all the peptides?

Not really, you can only view the genomic localization of the peptides that were present in the genomic mapping file (output from the first workflow).


Proteogenomics general

Can I use these workflows on datasets generated from our laboratory?

Question: Can I use these workflows on datasets generated from our laboratory?

Yes, the workflows can be used on other datasets as well. However, you will need to consider data acquisition and sample preparation methods so that the tool parameters can be adjusted accordingly.

Example histories for the proteogenomics tutorials

If you get stuck or would like to see what the results should look like, you can have a look at one of the following public histories:

Galaxy EU (usegalaxy.eu):

Galaxy Main (usegalaxy.org):

The workflows contain several Query tabular for text manipulation, is there a tutorial for that?

Question: The workflows contain several Query tabular for text manipulation, is there a tutorial for that?

Query tabular loads a tabular database and creates a sqlite database and tabular file. To learn more about SQL Queries - please look at this documentation.

The help section on the Query Tabular tool provides simple examples of both filtering the input tabular datasets, as well as examples of SQL queries. Query Tabular also incorporates regex functions that can be used queries. The PSM report datasets in these tutorials have fields that are lists of protein IDs.

Query Tabular help shows how to normalize those protein list fields so that we can perform operations by protein ID. See section: Normalizing by Line Filtering into 2 Tables in the tool help (below the tool in Galaxy).

What kind of variants are seen in the output?

Question: What kind of variants are seen in the output?

From this workflow we can see insertions, deletions, SNVs, or we will know whether it’s an intron, exon, splice junction etc.


General Questions

Can't find one of the tools for this tutorial?

To use the tools installed and available on the Galaxy server:

  1. At the top of the left tool panel, type in a tool name or datatype into the tool search box.
  2. Shorter keywords find more choices.
  3. Tools can also be directly browsed by category in the tool panel.

If you can’t find a tool you need for a tutorial on Galaxy, please:

  1. Check that you are using a compatible Galaxy server
    • Navigate to the overview box at the top of the tutorial
    • Find the “Supporting Materials” section
    • Check “Available on these Galaxies”
    • If your server is not listed here, the tutorial is not supported on your Galaxy server
    • You can create an account on one of the supporting Galaxies screenshot of overview box with available Galaxies section
  2. Use the Tutorial mode feature
    • Open your Galaxy server
    • Click on the icon on the top menu, this will open the GTN inside Galaxy.
    • Navigate to your tutorial
    • Tool names in tutorials will be blue buttons that open the correct tool for you
    • Note: this does not work for all tutorials (yet) gif showing how GTN-in-Galaxy works
  3. Still not finding the tool?

Running into an error?

When something goes wrong in Galaxy, there are a number of things you can do to find out what it was. Error messages can help you figure out whether it was a problem with one of the settings of the tool, or with the input data, or maybe there is a bug in the tool itself and the problem should be reported. Below are the steps you can follow to troubleshoot your Galaxy errors.

  1. Expand the red history dataset by clicking on it.
    • Sometimes you can already see an error message here

  2. View the error message by clicking on the bug icon

  3. Check the logs. Output (stdout) and error logs (stderr) of the tool are available:
    • Expand the history item
    • Click on the icon
    • Scroll down to the Job Information section to view the 2 logs:
      • Tool Standard Output
      • Tool Standard Error
    • For more information about specific tool errors, please see the Troubleshooting section
  4. Submit a bug report! If you are still unsure what the problem is.
    • Click on the bug icon
    • Write down any information you think might help solve the problem
      • See this FAQ on how to write good bug reports
    • Click Report button
  5. Ask for help!


Still have questions?
Gitter Chat Support
Galaxy Help Forum