Re: [galaxy-user] (no subject)

2013-09-11 Thread Jennifer Jackson

Hi Maria,

This message indicates that an error occurred on the cluster node 
processing the job. Normally these are not linked to inputs or tools and 
the general solution is to re-run the job. Please give this a try today 
- it is possible the error was linked to recent transient server issues.


If you continue to have problems after the re-run today, please submit a 
bug report from the error dataset, leaving inputs and outputs undeleted:

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

Best,

Jen
Galaxy team

On 9/11/13 12:38 PM, Maria Hoffman wrote:

Hello,

I am fairly new to galaxy and I am trying to use bowtie2 to map my 
reads against a custom genome (specifically a ribosomal RNA fasta 
file). I have formatted the file as suggested in the Galaxywiki ect 
and I am still getting the following message: Job output not returned 
by PBS: the output datasets were deleted while the job was running, 
the job was manually dequeued or there was a cluster error.


Any help would me much appreciated!

Maria


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Re: [galaxy-user] Data sources don't load in Firefox

2013-09-11 Thread Jennifer Jackson

Hi Carrie,

We are aware of this new issue with the Firefox 23.0.1 update. Using an 
alternate browser is recommended to avoid the problem with direct 
https->http connections, as several of Galaxy's "Get Data" tools/sources 
are impacted. Our team is reviewing solutions at a priority.


Hopefully this helps to confirm the issue, and our apologies for the 
current inconvenience,


Jen
Galaxy team

On 9/11/13 8:01 AM, Ganote, Carrie L wrote:

Hi List,

I'm trying to go through Galaxy 101, and the first step is halting me 
(UCSC Main table browser does nothing on click). I'm giving a 
presentation on how to use Galaxy, but the data sources do not load 
when using Firefox.


The tool click registers, because the history pane is minimized, but 
the URL is not invoked (no activity from browser). I went through my 
FF settings to see if I'm doing anything to block iframe loads. The 
funny thing is, though UCSC and BX don't load, but Biomart does - 
likely because it is not in an iframe but gets loaded as its own 
window. If I open in a new tab, it's fine.


These things load on Chrome, IE and Safari. A lot of my users use 
Firefox, however. I appreciate any insight into this.


Sincerely,

Carrie Ganote


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[galaxy-user] error message from Filezilla

2013-09-11 Thread Amit Pande
Hi,

I am getting the following error from the server :
Command:USER genebus...@googlemail.com
Response:331 Password required for genebus...@googlemail.com
Command:PASS ***
Response:530 Sorry, the maximum number of clients (3) for this user are
already connected.
Error:Critical error
Error:Could not connect to server.

Can you please help.

warm regards,
Amit.
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[galaxy-user] Data sources don't load in Firefox

2013-09-11 Thread Ganote, Carrie L
Hi List,

I'm trying to go through Galaxy 101, and the first step is halting me (UCSC 
Main table browser does nothing on click). I'm giving a presentation on how to 
use Galaxy, but the data sources do not load when using Firefox.

The tool click registers, because the history pane is minimized, but the URL is 
not invoked (no activity from browser). I went through my FF settings to see if 
I'm doing anything to block iframe loads. The funny thing is, though UCSC and 
BX don't load, but Biomart does - likely because it is not in an iframe but 
gets loaded as its own window. If I open in a new tab, it's fine.

These things load on Chrome, IE and Safari. A lot of my users use Firefox, 
however. I appreciate any insight into this.

Sincerely,

Carrie Ganote
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[galaxy-user] Questions about MEME & Sequence logo generator

2013-09-11 Thread Boaz Shaanan



Hi,


Has the MEME module been taken out of the main galaxy server? Assuming it'll be back, what's roughly a recommended number of sequences to feed into MEME? It has a limit on the sequences that it can digest but I don't know what it is. Likewise, what's this
 limit for the Sequence Logo Generator?


   Thanks,


              Boaz


 
 
Boaz Shaanan, Ph.D.

Dept. of Life Sciences  
Ben-Gurion University of the Negev  
Beer-Sheva 84105    
Israel  
    
E-mail: bshaa...@bgu.ac.il
Phone: 972-8-647-2220  Skype: boaz.shaanan  
Fax:   972-8-647-2992 or 972-8-646-1710
 
 










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[galaxy-user] (no subject)

2013-09-11 Thread Maria Hoffman
Hello,

I am fairly new to galaxy and I am trying to use bowtie2 to map my reads
against a custom genome (specifically a ribosomal RNA fasta file). I have
formatted the file as suggested in the Galaxywiki ect and I am still
getting the following message: Job output not returned by PBS: the output
datasets were deleted while the job was running, the job was manually
dequeued or there was a cluster error.

Any help would me much appreciated!

Maria
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Re: [galaxy-user] FASTQ joiner

2013-09-11 Thread Anton Nekrutenko
Lilach:

This tool works on unaligned reads in fastq format before they are mapped.
It is useful for merging mates together into a single read for QC
processing, filtering, and trimming.

Thanks!

anton


On Wed, Sep 11, 2013 at 4:34 AM, lilach noy  wrote:

> Hi all,
>
> Has anyone used FASTQ joiner with a file containing multi-mapped reads?
> I'm pretty sure i have reads mapped to several locations and i don't know
> what this tool does with it? will it locate the right map according to the
> paired read? will it use the first read location and ignore the rest or
> maybe it will exclude all multi-mapped reads prior to paring?
>
> Regards,
> Lilach
>
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>
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>
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>
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>
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Re: [galaxy-user] cannot download data to Galaxy

2013-09-11 Thread Nate Coraor
On Sep 11, 2013, at 9:56 AM, Elwood Linney wrote:

> 
> Hello,
> My connection with Galaxy online shutoff last night while I was transferring 
> data to it.  When I tried to connect again with Fetch this morning I was not 
> allowed and a message like "Sorry the maximum number of clients for this user 
> are already connected."
> 
> I have had what appears to be the bad habit of not logging off to Galaxy.  I 
> am working on the same data sets with three different computers, I only have 
> one login to Galaxy, so yes, I was logged in on 3 different computers.  When 
> I logged off of them, and tried to transfer data, I still got the same 
> message.
> 
> I realize people might be trying to get around the 250gb limit by having 
> multiple logins--I am not one of them, I am the only user on the three 
> computers I am using.  If not logging off when I leave the computer is a 
> problem to Galaxy, I will religiously log off each time I am not using the 
> computer (the computers are in three different rooms in my lab and my lab 
> consists of just me and a tech--I am the only one who knows the computer 
> login for both the computers and for Galaxy).
> 
> If I have created a problem by being "lazy", I apologize, but I have grown 
> dependent upon using Galaxy online and some new data just came in.

Hi Elwood,

This is not due to staying logged in to the web interface, I believe it's a bug 
in the FTP server that we're using.  I've restarted the server, could you let 
us know if you're still getting the maximum clients message if you try to 
connect?

--nate

> 
> Sincerely,
> 
> Elwood Linney
> Professor of Molecular Genetics and Microbiology
> Duke University Medical Center
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Re: [galaxy-user] error message from Filezilla

2013-09-11 Thread Nate Coraor
On Sep 11, 2013, at 7:48 AM, Amit Pande wrote:

> Hi,
> 
> I am getting the following error from the server :
> Command:USER genebus...@googlemail.com
> Response:331 Password required for genebus...@googlemail.com
> Command:PASS ***
> Response:530 Sorry, the maximum number of clients (3) for this user are 
> already connected.
> Error:Critical error
> Error:Could not connect to server.
> 
> Can you please help.

Hi Amit,

Please give it a try now, I've restarted the FTP server (I believe this is due 
to a bug in the server).

--nate

> 
> warm regards,
> Amit.
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> please use the interface at:
> 
>  http://lists.bx.psu.edu/
> 
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[galaxy-user] cannot download data to Galaxy

2013-09-11 Thread Elwood Linney
Hello,
My connection with Galaxy online shutoff last night while I was
transferring data to it.  When I tried to connect again with Fetch this
morning I was not allowed and a message like "Sorry the maximum number of
clients for this user are already connected."

I have had what appears to be the bad habit of not logging off to Galaxy.
I am working on the same data sets with three different computers, I only
have one login to Galaxy, so yes, I was logged in on 3 different
computers.  When I logged off of them, and tried to transfer data, I still
got the same message.

I realize people might be trying to get around the 250gb limit by having
multiple logins--I am not one of them, I am the only user on the three
computers I am using.  If not logging off when I leave the computer is a
problem to Galaxy, I will religiously log off each time I am not using the
computer (the computers are in three different rooms in my lab and my lab
consists of just me and a tech--I am the only one who knows the computer
login for both the computers and for Galaxy).

If I have created a problem by being "lazy", I apologize, but I have grown
dependent upon using Galaxy online and some new data just came in.

Sincerely,

Elwood Linney
Professor of Molecular Genetics and Microbiology
Duke University Medical Center
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[galaxy-user] GATK error Argument with name 'T' isn't defined

2013-09-11 Thread Erica Westerman
Aloha. I am using GATK in Galaxy for the first time, on a local Galaxy server, 
and when I try to run Count Covariates I get the error: ERROR stack trace 
org.broadinstitute.sting.commandline.InvalidArgumentException: Argument with 
name 'T' isn't defined. at org.broadinstitute.s

I have looked at the GATK Count Covariates command line, and it looks to me 
like the argument with name 'T' is not a place where I need to input a file, 
but is where the Count Covariates software information goes. I get this same 
error when trying to run Realigner Target Creator.

I wondered if this might be something that could be simply fixed by 
reinstalling the wrappers for GATK, or something along those lines?
  Thank you!


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[galaxy-user] extension of read length

2013-09-11 Thread Tobias Hohenauer

Dear all,

I am working on an MNAse-Seq experiment with 50bp single end reads. To 
identify nucleosome positions, I read that one needs to extend the 
single reads to approximately the length of nucleosome protected DNA, 
being approximately 150bp.


Is there a way in Galaxy to extend 50bp reads to 150bp length, lets say 
from a .BAM file with mapped reads?

Of course any other comment on this topic is much appreciated!

Thank you very much,

Tobias

--
Tobias Hohenauer, PhD
GCNA, Disease Mechanism Research Core
RIKEN Brain Science Institute
2-1 Hirosawa, Wako-shi
351-0198 Japan

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[galaxy-user] FASTQ joiner

2013-09-11 Thread lilach noy
Hi all,

Has anyone used FASTQ joiner with a file containing multi-mapped reads?
I'm pretty sure i have reads mapped to several locations and i don't know
what this tool does with it? will it locate the right map according to the
paired read? will it use the first read location and ignore the rest or
maybe it will exclude all multi-mapped reads prior to paring?

Regards,
Lilach
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