Re: [galaxy-user] Error installing MACS on local Galaxy

2012-10-18 Thread Jerzy Dyczkowski

Hi Jennifer,

I am now trying to run MACS 1.3.7.1. in Galaxy.
I also ran python setup.py install and set variables $PATH and 
$PYTHONPATH for the commandline run. Nevertheless, MACS gives error: 
/ImportError: No module named MACS.OptValidator/
I checked - library OptValidator.py exists in the file system, and path 
to the folder is both in $PATH and $PYTHONPATH

Any ideas?

best regards,

Jerzy



On 10/17/2012 04:18 PM, Jennifer Jackson wrote:

Hello Jerzy,

The MACS wrapper in Galaxy currently supports version 1.3, which 
explains the problems with 1.4. Tool dependencies are noted on this wiki:

http://wiki.g2.bx.psu.edu/Admin/Tools/Tool%20Dependencies

For the other errors, are you trying to run MACS on the command line 
or within Galaxy? For command line, some environment variables need to 
be set up, the MACS documentation has the details:

http://liulab.dfci.harvard.edu/MACS/INSTALL.html

Hopefully this helps,

Jen
Galaxy team

On 10/17/12 2:09 AM, Jerzy Dyczkowski wrote:

Hello,

I cannot run MACS on the local Galaxy. When I install MACS version 1.4.,
it gives error something like cannot find macs. When I install version
1.3.7.1 it gives error /line 34, in module from MACS.OptValidator
import opt_validate ImportError: No module named MACS.OptValidator/
I sourced PATH to the directory with this module. Any ideas?

best regards,

Jerzy

--
Dr Jerzy Dyczkowski
Bioinformatician
Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
Grisebachstr. 5
D-37077 Göttingen
Email:jerzy.dyczkow...@eni-g.de
Phone: +49 (0)551 39-12352



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--
Dr Jerzy Dyczkowski
Bioinformatician
Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
Grisebachstr. 5
D-37077 Göttingen
Email: jerzy.dyczkow...@eni-g.de
Phone: +49 (0)551 39-12352

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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
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[galaxy-user] Error installing MACS on local Galaxy

2012-10-17 Thread Jerzy Dyczkowski

Hello,

I cannot run MACS on the local Galaxy. When I install MACS version 1.4., 
it gives error something like cannot find macs. When I install version 
1.3.7.1 it gives error /line 34, in module from MACS.OptValidator 
import opt_validate ImportError: No module named MACS.OptValidator/

I sourced PATH to the directory with this module. Any ideas?

best regards,

Jerzy

--
Dr Jerzy Dyczkowski
Bioinformatician
Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
Grisebachstr. 5
D-37077 Göttingen
Email: jerzy.dyczkow...@eni-g.de
Phone: +49 (0)551 39-12352

___
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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:

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[galaxy-user] Upload data to local Galaxy by copying them to the file folder

2012-10-12 Thread Jerzy Dyczkowski

Hello,

How to put data to the local Galaxy server via ftp, ssh or copying 
directly to some subfolder in galaxy-dist?


We installed a local Galaxy instance and it is running. Manual uploading 
files from user PCs is slow due to less than perfect connections in the 
local network. We would prefer uploading large files by ssh from the 
central cluster to the server on which Galaxy is running. I can conect 
to the Galaxy server and Galaxy folder structure, however, I cannot find 
where to put files. Are they all renamed and coded as something like: 
galaxy-dist/database/files/000/dataset_38.dat ?


The option of uploading via ftp on main.g2.bx.psu.edu is absent in local 
Galaxy distribution.


best regards,

Jerzy
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[galaxy-user] Extracting number of reads from Bowtie analysis

2012-03-12 Thread Jerzy Dyczkowski

Hello, I am new here!

I am aligning Solexa files to genome using tool: NGS: Mapping: Map with 
Bowtie for Illumina.


My question: What is the most easy way to check the number of aligned 
reads in the output from above?


I couldn't find this number directly. I found a way, but it looks 
circular and unoptimal: to run Bowtie with option: put umapped reads 
into the file, download the file, open it, count reads, subtract from 
reads in the original file. However, downloading large files is 
time-consuming, and I am sure the easier way is somewhere.


Further question: good link to help on how to improve number of reads 
from ChIP study aligned to mouse genome would be also appreciated.


best regards,

Jerzy


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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:

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