[galaxy-user] Error in annotation tools

2013-05-09 Thread Gema Sanz Santos
Hello,

I'm using Nebula and when I try to use the annotation tools (genomic
annotation and gene annotation in NGS annotation menu) I got always this
error despite of the bed file that I use:

An error occurred running this job:Unable to run this job due to a cluster
error

Could you indicate me how to solve this?

Regards,
Gema

From:  Jennifer Jackson j...@bx.psu.edu
Date:  Wednesday, May 8, 2013 5:36 AM
To:  Elwood Linney ellin...@gmail.com
Cc:  galaxy-u...@bx.psu.edu
Subject:  Re: [galaxy-user] problems with Tophat


 Hello Elwood,
 
 The public Main Galaxy server was very busy this weekend this likely
contributed to the problems you were having with loaded and possibly with
job execution. 
 
 First, be sure that you are loading with FTP and confirming that loading is
successful with a client during this time. This also permits interrupted
loads can be restarted as necessary.
 http://wiki.galaxyproject.org/FTPUpload
 
 For the Tophat job, there were some known job failures related to load. I
would restart the job and see if a new run resolves the issue. If the
problem is persistent, please submit the new error as a bug report and we
can take a closer look. Be sure to leave all inputs and both Tophat runs
active (undeleted) if you submit a bug report, as a history is often very
helpful/necessary when diagnosing a problem.
 
 Sorry that you were having problems, but hopefully these can be resolved
quickly.
 
 Best,
 
 Jen
 Galaxy team
 
 
 
 
On 5/7/13 6:34 AM, Elwood Linney wrote:
 
 
  
  
  
  
 Hello,  I have successfully used the public server for processing RNAseq data
 but I have run into some problems this weekend.  And this weekend there were
 various times when I would get a message that Galaxy was not available.
  
  Specifically, I received some new 50bp single-ended RNAseq data and proceeded
 to process it through the public server as I have done successfully before.
  
  I concatenated it the subfiles into one fastq file, transferred it to Galaxy,
 groomed it just to be safe, looked at its quality and did not have to trim it
 and then I passed it on to Tophat. [all in the same manner that had worked for
 me before]
  
  It consisted of 4, approximately 15gb files.  While i was moving these files
 individuallly into the Tophat stage this weekend  there were interruptions in
 the availability of Galaxy.  I waited during the weekend, one set of the 4
 Tophat files for one of the 4 datasets was processed but then 1 file that I
 had processed during the interruption turned out to have errors, so I deleted
 it and re-entered it, another set was processing overnight and then it turned
 out to have errors.  So thinking that maybe 3 of the 4 sets for some reason
 had problems, I deleted them, re entered them.  One was going overnight and
 into the day and this morning it had errors.
  
  Since i am not sure how to read these errors, I am at a loss as to what is
 happening, particularly since one of my files was successfully processed
 through Tophat.  This is the readout for one of the 4 Tophat files that were
 in error.  Any advice on this would be welcome since I hope to soon have a
 64gb ram computer with 12 cores to transfer Galaxy to.
  
  
  43: Tophat for Illumina on data 8: accepted_hits
 error
  An error occurred with this dataset: TopHat v1.4.0 tophat -p 8
 /galaxy/data/danRer7/bowtie_index/danRer7
 /galaxy/main_pool/pool7/files/006/143/dataset_6143636.dat Exception in thread
 Thread-1: Traceback (most recent call last): File
 /usr/global/python/2.6.5/lib/python2.6/threading.py, l
  
  
  
  Sincerely,
  
  
  Elwood Linney
  
  Duke University Medical Center
  
  
  
  
 
  
  
  
  
  
  
  
   
  
 ___
 The Galaxy User list should be used for the discussion of
 Galaxy analysis and other features on the public server
 at usegalaxy.org.  Please keep all replies on the list by
 using reply all in your mail client.  For discussion of
 local Galaxy instances and the Galaxy source code, please
 use the Galaxy Development list:
 
   http://lists.bx.psu.edu/listinfo/galaxy-dev
 
 To manage your subscriptions to this and other Galaxy lists,
 please use the interface at:
 
   http://lists.bx.psu.edu/
 
 To search Galaxy mailing lists use the unified search at:
 
   http://galaxyproject.org/search/mailinglists/
  
 
 
-- 
Jennifer Hillman-Jackson
Galaxy Support and Training
http://galaxyproject.org
 
___ The Galaxy User
list should be used for the discussion of Galaxy analysis and other features
on the public server at usegalaxy.org.  Please keep all replies on the list
by using reply all in your mail client.  For discussion of local Galaxy
instances and the Galaxy source code, please use the Galaxy Development
list:  http://lists.bx.psu.edu/listinfo/galaxy-dev To manage your
subscriptions to this and other Galaxy lists, please use the interface at:
http://lists.bx.psu.edu/ To 

[galaxy-user] FW: Error in annotation tools

2013-05-09 Thread Gema Sanz Santos
I edit:

Actually I canĀ“t do anything in nebula server, even upload data, I got the
cluster error all the time

From:  Gema Sanz Santos ge2sa...@gmail.com
Date:  Thursday, May 9, 2013 1:14 PM
To:  Jennifer Jackson j...@bx.psu.edu
Cc:  galaxy-u...@bx.psu.edu
Subject:  Error in annotation tools

Hello,

I'm using Nebula and when I try to use the annotation tools (genomic
annotation and gene annotation in NGS annotation menu) I got always this
error despite of the bed file that I use:

An error occurred running this job:Unable to run this job due to a cluster
error

Could you indicate me how to solve this?

Regards,
Gema




___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

  http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

  http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

  http://galaxyproject.org/search/mailinglists/

[galaxy-user] Filter Fastq

2013-05-09 Thread Casey,Richard
Hi,

We have two Filter FASTQ jobs running on the Galaxy public server.  Both jobs 
have been running for more than four days.  This seems like an excessive amount 
of runtime.  Do Filter FASTQ jobs normally take this long to run?



Richard


___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

  http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

  http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

  http://galaxyproject.org/search/mailinglists/


Re: [galaxy-user] Filter Fastq

2013-05-09 Thread Peter Cock
On Thu, May 9, 2013 at 12:27 PM, Casey,Richard
richard.ca...@colostate.edu wrote:
 Hi,

 We have two Filter FASTQ jobs running on the Galaxy public server.
 Both jobs have been running for more than four days.  This seems like
 an excessive amount of runtime.  Do Filter FASTQ jobs normally take
 this long to run?

Which FASTQ filtering tool exactly are you referring too? The one called
Filter FASTQ reads by quality score and length in the left hand column,
tool ID fastq_filter?

How big were the input files?

Peter
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

  http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

  http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

  http://galaxyproject.org/search/mailinglists/


[galaxy-user] nebula problem

2013-05-09 Thread Gema Sanz Santos
Hello,

I'm using Nebula and when I try to use the annotation tools (genomic
annotation and gene annotation in NGS annotation menu) I got always this
error despite of the bed file that I use:

An error occurred running this job:Unable to run this job due to a cluster
error

I also got this error message for everything that I try, even upload data
sets (which I can not upload anymore)

Could you indicate me how to solve this?

Regards,
Gema



___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

  http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

  http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

  http://galaxyproject.org/search/mailinglists/

[galaxy-user] How to analyze the Encode RNA-seq data from UCSC genome browser with Galazy

2013-05-09 Thread Santagostino Marco
Dear Sir/Madam,

I am new at Galaxy. I need to define if a set loci ( about 700) is
transcribed, i.e. these loci overlap with those reported in the Encode
RNA-seq data. The track contains several tables, can you please suggest me
how to proceed? do I need to download all the tables from UCSC table
browser and then upload/send them to Galaxy? Is there a way to refer only
to the Encode RNA-seq track without downloading the whole table set?
I have the coordinates of each one of my loci, from those I can obtain the
sequences. I intended to use the Public Galaxy Main Instance.

Thank you,

Marco Santagostino



-- 
Marco Santagostino, PhD
Laboratorio di Biologia Molecolare e Cellulare
Dipartimento di Biologia e Biotecnologie, University of Pavia
Ferrata street, 9 - 27100 Pavia, Italy
Tel.: +39 0382 985540
Fax: +39 0382 528496
e-mail: marco.santagost...@unipv.it
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

  http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

  http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

  http://galaxyproject.org/search/mailinglists/

Re: [galaxy-user] Filter Fastq

2013-05-09 Thread Jennifer Jackson

Hi Richard,

The public Main Galaxy server has been very busy lately. To let you 
know, the size of the job will not determine when a job will start, only 
the time it was started/queued with respect to other user's jobs also 
queued and in less common circumstances the specific type of job (that 
requires a particular cluster node type - this was not the case for your 
job). How long a job executes (will be in the yellow running state) is 
related to the size of the inputs, the type of job, and parameters.


I see that these have now failed with a cluster error - please re-run 
the failed jobs one more time. If you continue to have problems, please 
submit one of the error datasets as a bug report, leaving all 
inputs/outputs undeleted.

http://wiki.galaxyproject.org/Support#Reporting_tool_errors

Very sorry that this was causing confusion. And thanks Peter for the help!

Jen
Galaxy team

On 5/9/13 4:27 AM, Casey,Richard wrote:

Hi,

We have two Filter FASTQ jobs running on the Galaxy public server.  Both jobs 
have been running for more than four days.  This seems like an excessive amount 
of runtime.  Do Filter FASTQ jobs normally take this long to run?



Richard


___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

   http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

   http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

   http://galaxyproject.org/search/mailinglists/


--
Jennifer Hillman-Jackson
Galaxy Support and Training
http://galaxyproject.org

___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

 http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

 http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

 http://galaxyproject.org/search/mailinglists/


Re: [galaxy-user] nebula problem

2013-05-09 Thread Jennifer Jackson

Hi Gema,

This is the support email for the public Main Galaxy instance at 
usegalaxy.org (https://main.g2.bx.psu.edu/).


To get help with this other public Galaxy instance, it would be best to 
contact them directly for help.

http://wiki.galaxyproject.org/PublicGalaxyServers

They have two troubleshooting contacts listed at their welcome page here:
http://nebula.curie.fr/

Good luck,

Jen
Galaxy team

On 5/9/13 8:38 AM, Gema Sanz Santos wrote:

Hello,

I'm using Nebula and when I try to use the annotation tools (genomic 
annotation and gene annotation in NGS annotation menu) I got always 
this error despite of the bed file that I use:


An error occurred running this job:/Unable to run this job due to a 
cluster error/

/
/
I also got this error message for everything that I try, even upload 
data sets (which I can not upload anymore)


Could you indicate me how to solve this?

Regards,
Gema



___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

   http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

   http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

   http://galaxyproject.org/search/mailinglists/


--
Jennifer Hillman-Jackson
Galaxy Support and Training
http://galaxyproject.org

___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

  http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

  http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

  http://galaxyproject.org/search/mailinglists/

Re: [galaxy-user] How to analyze the Encode RNA-seq data from UCSC genome browser with Galazy

2013-05-09 Thread Jennifer Jackson

Hi Marco,

Each RNA-seq study in the ENCODE project may have variable coverage, but 
if the goal is to identify overlapping regions with gene annotations 
targeted by the ENCODE project, the GENCODE Genes track is most likely 
the one you are looking for.


Review the contents of the track at the ENCODE hub at UCSC by going to 
their web site http://genome.ucsc.edu, clicking into Genomes, the target 
genome (hg19?), then scroll down to the track group Gene and Gene 
Predictions. Click on the track Gencode genes to read about how it is 
constructed, what the content options are, and how these relate to 
ENCODE builds. You can follow more links in the description to the 
subtracks (for example, in hg19, Version 14 is the most current), and 
describe schema will take you into the Table Browser where the actual 
format of the data table can be reviewed. Tools - Table Browser will 
bring you to a form where the table can be extracted and sent to Galaxy, 
it is the same form found in Galaxy under Get data - UCSC Main.


If you start this browser process while still logged into Galaxy from 
the history you want to import the data in to, you can extract directly 
from here, making sure that Galaxy is checked (it will be by default) 
next to the output format: BED section of the form. Or, you can simply 
explore, and once you know what tracks/tables you are interested in, go 
through the Galaxy tool Get data - UCSC Main.


You may know this already, but the core hub for ENCODE is at:
http://genome.ucsc.edu/ENCODE/index.html

Basic examples that show how to extract data from UCSC and use 
coordinate overlap comparison tools can be found at:

https://main.g2.bx.psu.edu/u/aun1/p/galaxy101
https://main.g2.bx.psu.edu/u/galaxyproject/p/using-galaxy-2012 (protocol 1)

More screencasts/tutorials are at:
http://wiki.galaxyproject.org/Learn/Screencasts
https://main.g2.bx.psu.edu/page/list_published

Hopefully this helps,

Jen
Galaxy team

On 5/9/13 11:01 AM, Santagostino Marco wrote:

Dear Sir/Madam,

I am new at Galaxy. I need to define if a set loci ( about 700) is 
transcribed, i.e. these loci overlap with those reported in the Encode 
RNA-seq data. The track contains several tables, can you please 
suggest me how to proceed? do I need to download all the tables from 
UCSC table browser and then upload/send them to Galaxy? Is there a way 
to refer only to the Encode RNA-seq track without downloading the 
whole table set?
I have the coordinates of each one of my loci, from those I can obtain 
the sequences. I intended to use the Public Galaxy Main Instance.


Thank you,

Marco Santagostino



--
Marco Santagostino, PhD
Laboratorio di Biologia Molecolare e Cellulare
Dipartimento di Biologia e Biotecnologie, University of Pavia
Ferrata street, 9 - 27100 Pavia, Italy
Tel.: +39 0382 985540
Fax: +39 0382 528496
e-mail: marco.santagost...@unipv.it mailto:marco.santagost...@unipv.it


___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

   http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

   http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

   http://galaxyproject.org/search/mailinglists/


--
Jennifer Hillman-Jackson
Galaxy Support and Training
http://galaxyproject.org

___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using reply all in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

  http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

  http://lists.bx.psu.edu/

To search Galaxy mailing lists use the unified search at:

  http://galaxyproject.org/search/mailinglists/