[galaxy-user] the original subject for the thread

2011-06-14 Thread David Wang
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Subject: galaxy-user Digest, Vol 60, Issue 14

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Today's Topics:

   1. SAM to bigbed (Aleks Schein)
   2. Re: SAM to bigbed (Jennifer Jackson)
   3. GenBank Submission - How to Generate Fasta (not   fastq) files
  (John David Osborne)


--

Message: 1
Date: Mon, 13 Jun 2011 18:42:45 +0200
From: Aleks Schein al...@mb.au.dk
To: galaxy-user@lists.bx.psu.edu
Subject: [galaxy-user] SAM to bigbed
Message-ID: 20110613184245.14175jqs5ml9m...@webmail.nfit.au.dk
Content-Type: text/plain; charset=ISO-8859-1; DelSp=Yes;
format=flowed

Hi,
Is it possible to generate a bigbed or bigwig file from SAM (or BAM)  
file using Galaxy? It looks like there is such option in the full  
version of SAMTools, but I have no appropriate machine to run SAMTools.

Thanks,

Aleks


--

Message: 2
Date: Mon, 13 Jun 2011 10:03:04 -0700
From: Jennifer Jackson j...@bx.psu.edu
To: Aleks Schein al...@mb.au.dk
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] SAM to bigbed
Message-ID: 4df642c8.3070...@bx.psu.edu
Content-Type: text/plain; charset=ISO-8859-1; format=flowed

Hi Aleks,

There is no function in Galaxy for this in one step, but there are other

options:

1) only convert to BAM and view at UCSC that way, if visualization is 
your goal. This preserves the primary sequence information in the file 
so that it can be viewed/used in downstream analysis.

2) use Generate Pileup then Pileup-to-Interval. Interval can be 
changed to BED using the pencil icon (you may need to arrange column 
order first to meet spec, as BED columns must be in a specific order, as

defined on any of the tools involving BED files). The resulting BED file

can then be condensed by BED-to-bigBed. This loses the primary 
sequence information - only coordinates are retained - may or may not be

desirable.

Hopefully this helps,

Jen
Galaxy team

On 6/13/11 9:42 AM, Aleks Schein wrote:
 Hi,
 Is it possible to generate a bigbed or bigwig file from SAM (or BAM)
 file using Galaxy? It looks like there is such option in the full
 version of SAMTools, but I have no appropriate machine to run
SAMTools.

 Thanks,

 Aleks
 ___
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-- 
Jennifer Jackson
http://usegalaxy.org/
http://galaxyproject.org/


--

Message: 3
Date: Mon, 13 Jun 2011 13:34:11 -0500
From: John David Osborne ozb...@uab.edu
To: galaxy-u...@bx.psu.edu galaxy-u...@bx.psu.edu
Subject: [galaxy-user] GenBank Submission - How to Generate Fasta (not
fastq) files
Message-ID:
27f664987feadb4ea29031f58bc42b3e02144...@uabexmbs5.ad.uab.edu
Content-Type: text/plain; charset=iso-8859-1

I still haven't found an easy solution to this problem and I am afraid
I'm going to have to write one my own - which makes little sense as I
bet this has been solved thousands of times!

Can anybody point me to a script/software to convert a samtools pileup
file into a fasta consensus file? It would be nice to set coverage
thresholds, etc... but I'll take anything I can work with.

The best google could do for me was this:
http://biostar.stackexchange.com/questions/1389/how-to-generate-a-consen

[galaxy-user] can I merge histories?

2011-06-14 Thread Robert Curtis Hendrickson
Folks,

Is there some way I can merge histories?

I ran a workflow on 3 different samples in one history, each time putting them 
in a different history with the same name. However, Galaxy created 3 new 
histories, each with the same name! But I need the data in the same history to 
compare and contrast it.

Thanks,
Curtis

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[galaxy-user] software request

2011-06-14 Thread Christopher Balakrishnan

Hi there,

I noticed on Seqanswers there was a post inquiring about the potential  
addition of DE-Seq (Anders  Huber) to the growing stack of tools  
available in galaxy.


I for one would love to see this integrated.
I typically use it in combination with HT-Seq, a set of python scripts  
also from Simon Anders. This simply has the functionality of  
converting a SAM alignment to simple counts of reads per transcript  
across the genome. Probably there are tools is Galaxy that do a  
similar thing. In any case I think many people are using TopHat - HT- 
Seq - DE-Seq for analysis of RNAseq data so it would be great if DE- 
Seq were supported in Galaxy


My two cents..

Thanks for all your great work!

Chris
Christopher Balakrishnan
Institute for Genomic Biology
University of Illinois
1206 W. Gregory Drive MC-195
Urbana, IL 61801
phone: 617-905-2910
http://myweb.ecu.edu/balakrishnanc

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Re: [galaxy-user] software request

2011-06-14 Thread Philippe Lefebvre

Hi Chris
You may find DESeq at the Galaxy website http://galaxy.fml.mpg.de/

Le 14/06/2011 19:28, Christopher Balakrishnan a écrit :

Hi there,

I noticed on Seqanswers there was a post inquiring about the potential 
addition of DE-Seq (Anders  Huber) to the growing stack of tools 
available in galaxy.


I for one would love to see this integrated.
I typically use it in combination with HT-Seq, a set of python scripts 
also from Simon Anders. This simply has the functionality of 
converting a SAM alignment to simple counts of reads per transcript 
across the genome. Probably there are tools is Galaxy that do a 
similar thing. In any case I think many people are using TopHat - 
HT-Seq - DE-Seq for analysis of RNAseq data so it would be great if 
DE-Seq were supported in Galaxy


My two cents..

Thanks for all your great work!

Chris
Christopher Balakrishnan
Institute for Genomic Biology
University of Illinois
1206 W. Gregory Drive MC-195
Urbana, IL 61801
phone: 617-905-2910
http://myweb.ecu.edu/balakrishnanc

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--
Best regards/Cordialement

__

Philippe Lefebvre, Ph.D.
Directeur de Recherche INSERM
INSERM UMR 1011-Bâtiment JK
Université Lille-Nord de France; Faculté de Médecine de Lille-Pôle Recherche
Boulevard du Professeur Leclerc
59045 Lille cedex
France
Tel +33.3.20974220
Cell. Phone +33.6.87829495
Fax +33.3.20974201

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Re: [galaxy-user] working collaboratively in a history: How To?

2011-06-14 Thread Jennifer Jackson

Hi Curtis,

It may be helpful if I first help to clarify how the 
history/dataset/workflows are organized.


1 - When a dataset is moved (through either method), internal linkage is 
not preserved.


You could resolve this in two ways:

 a - By annotating where the moved result dataset came from. One 
suggestion for this would be to add in name of the other history - 
unique history naming would be advised - and keeping that history around 
for reference/traceability.


 b - Putting all of the work in the same history (best solution, 
especially if you are going to be creating workflows)


2 - When a history is shared, the other user creates a clone of your 
history as it exists when it is first imported by them. To conserve 
space, the underlying datasets are kept as a single file on the file 
system (as long as they are unchanged), but no user accessible linkage 
exists between the two histories after the clone is created. Changes in 
one history do not effect the other. If you want to share new results, 
have your collaborator import the history again. Naming imported 
histories in some way that will distinguish between revisions would be a 
good idea (unique names for histories is advised, shared or not).


3 - There are no roles that will allow two users to actively work on the 
same history. Also, it is not recommended to share the same 
user/password in an attempt to work in the same space - unexpected 
results may occur (not bugs, just internal tracking conflicts).


Hopefully this helps to address your questions about sharing histories, 
but please let us know if something was missed or is still unclear.


For searching the Galaxy wiki, specificity can be achieved by using a 
site key plus the search term. This is the Google link with the Galaxy 
wiki site key included. After clicking into Google with this link, add 
in your search term(s) after the site key and submit.


http://www.google.com/search?q=site%3Ahttp%3A%2F%2Fbitbucket.org%2Fgalaxy%2Fgalaxy-central%2Fwiki

This link is also documented at the very bottom of the Galaxy wiki home 
page:

https://bitbucket.org/galaxy/galaxy-central/wiki/Home


Thanks for using Galaxy!

Jen



--
Jennifer Jackson
http://usegalaxy.org/
http://galaxyproject.org/
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[galaxy-user] Error running latest Galaxy Distribution: numpy.dtype exception

2011-06-14 Thread Michael Steder
I'm just following the documentation here: 
https://bitbucket.org/galaxy/galaxy-central/wiki/GetGalaxy

And I ran into the following error:

$ hg clone https://bitbucket.org/galaxy/galaxy-dist
$ cd galaxy-dist
$ sh run.sh
Fetch successful.
Traceback (most recent call last):
  File /Users/steder/GO/GoGalaxy/galaxy-dist/lib/galaxy/web/buildapp.py, line 
81, in app_factory
from galaxy.app import UniverseApplication
  File /Users/steder/GO/GoGalaxy/galaxy-dist/lib/galaxy/app.py, line 11, in 
module
from galaxy.tools.imp_exp import load_history_imp_exp_tools
  File 
/Users/steder/GO/GoGalaxy/galaxy-dist/lib/galaxy/tools/imp_exp/__init__.py, 
line 6, in module
from galaxy.web.base.controller import UsesHistory
  File 
/Users/steder/GO/GoGalaxy/galaxy-dist/lib/galaxy/web/base/controller.py, line 
12, in module
from galaxy.visualization.tracks.data_providers import get_data_provider
  File 
/Users/steder/GO/GoGalaxy/galaxy-dist/lib/galaxy/visualization/tracks/data_providers.py,
 line 16, in module
from bx.arrays.array_tree import FileArrayTreeDict
  File numpy.pxd, line 119, in init bx.arrays.array_tree 
(lib/bx/arrays/array_tree.c:11323)
ValueError: numpy.dtype does not appear to be the correct type object

I was able to run the previous stable version of Galaxy.  Is there something I 
can do to get galaxy-dist running?

Should I be running galaxy-central instead?

~Mike
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