Re: [galaxy-dev] apache proxy

2015-02-18 Thread Dannon Baker
Hey Thon,

I'd probably recommend using a simple supervisord (http://supervisord.org/)
configuration to do this.   Here's a link to some great reference material
that might help you out:
https://wiki.galaxyproject.org/Events/GCC2014/TrainingDay/AdminWalkthrough#Configure_supervisord

-Dannon

On Wed Feb 18 2015 at 11:11:36 AM Michael Thon mike.t...@gmail.com wrote:

 If I use apache to proxy connections to the galaxy run.sh process, what is
 the best way to launch galaxy at boot time?  Can apache do it?

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Re: [galaxy-dev] problem with latest toolshed devteam cuffmerge wrapper multi-select

2015-02-18 Thread Nikhil Joshi
And, yes, all of the gtf files have the correct database build associated
with them.

On Wed, Feb 18, 2015 at 6:29 PM, Nikhil Joshi najo...@ucdavis.edu wrote:

 Hi all,

 We run our own custom galaxy instance in the Amazon Cloud and I am
 updating our instance with the latest toolshed files. For cuffmerge, in
 past revisions, we would just have a button to add another GTF input.
 However, this latest one (10:b6e3849293b1
 https://toolshed.g2.bx.psu.edu/repository/view_changelog?id=84bbebf45888f374)
 that has been replaced with a multi-select. We also have a few built-in
 genomes that we use with cuffmerge. When I choose the first GTF file (using
 locally cached sequence data) it will populate the reference genome
 correctly with our built-in genomes. However, once I choose more than one
 GTF file, I get one of two errors:

   No reference genome is available for the build associated with the
 selected input dataset
 OR
  An invalid option was selected, please verify

 The built-in genomes are definitely there and available for cuffmerge, but
 for some reason choosing more than one GTF file in the multi-select causes
 an error. Is this a bug or am I doing something wrong?

 - Nik.



 --
 Nikhil Joshi
 Bioinformatics Analyst/Programmer
 UC Davis Bioinformatics Core
 http://bioinformatics.ucdavis.edu/
 najoshi -at- ucdavis -dot- edu
 530.752.2698 (w)




-- 
Nikhil Joshi
Bioinformatics Analyst/Programmer
UC Davis Bioinformatics Core
http://bioinformatics.ucdavis.edu/
najoshi -at- ucdavis -dot- edu
530.752.2698 (w)
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Re: [galaxy-dev] Hooking a dataset full deletion

2015-02-18 Thread Raffaele Montella
Thanks Dannon!
Actually I’d like to avoid code hacking enforcing NTCC (no touch core code!).
Anyway, if there is no other way I’ll share the hack with the community, maybe 
could be part of next core improvements.
Bests,
— Raffaele

 On 18 Feb 2015, at 07:19, Dannon Baker dannon.ba...@gmail.com wrote:
 
 There isn't a hook that already exists for this, but if this is for a custom 
 instance and you're looking to hack something in, you could add extra logic 
 to lib/galaxy/managers/hdas.py in the 'purge' method.  Let me know if you 
 need more information, good luck!
 
 -Dannon
 
 On Tue Feb 17 2015 at 6:37:52 PM Raffaele Montella 
 raffaele.monte...@uniparthenope.it 
 mailto:raffaele.monte...@uniparthenope.it wrote:
 Hi,
 
 I need to perform some actions when a dataset if fully deleted.
 Does it exist a hook in datatype definition to do that?
 Thanks,
   Raffaele
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Re: [galaxy-dev] fastq format recognition

2015-02-18 Thread Michael Thon
Thanks Martin - allow_library_path_paste did the job.
Mike

 On Feb 18, 2015, at 6:14 AM, Martin Čech mar...@bx.psu.edu wrote:
 
 Hello Mike,
 
 you probably want to set library_import_dir or allow_library_path_paste in 
 the config.
 Details here: 
 https://wiki.galaxyproject.org/Admin/DataLibraries/UploadingLibraryFiles
 
 Martin
 
 On Tue Feb 17 2015 at 11:40:37 PM Michael Thon mike.t...@gmail.com wrote:
 
  On Feb 13, 2015, at 1:35 PM, Peter Cock p.j.a.c...@googlemail.com wrote:
 
  On Fri, Feb 13, 2015 at 12:08 PM, Michael Thon mike.t...@gmail.com wrote:
  I have a new galaxy installation on my server.  I uploaded two fastq files 
  and now I'm trying to run trimmomatic and fastqc. In both cases I am 
  presented with a drop down list of fastq files to select from but the 
  lists are empty.  I double checked the fastq file attributes and they are 
  both set to fastq. Any ideas what's wrong?
 
 
  You probably need to change the format to the more specific
  fastqsanger datatype (FASTQ using the Sanger encoding).
 
  It may be time for Galaxy to change their default, since the old
  Solexa and Illumina variants are no longer widely used.
 
  Another question: I have fastq files already on the same server as the 
  galaxy installation.  How can I get them into galaxy? I have not set up 
  ftp yet. Can I move them into a data directory somewhere?
 
  One option is to import them into a library (which can link to the
  files rather than coping them). Are you a Galaxy administrator?
 
  Peter
 
 I just tried adding them to a library.  On the library admin page there is an 
 option to upload files or to import data from my history.  There is no option 
 to link to files on the filesystem.  Does this need to be activated in the 
 config somewhere?
 Thanks
 
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