Hello,
I am trying to extract sequences from a FASTA file containing genomic
information. The coordinates are in a tab-delimited format, which is recognized
as BED format by Galaxy (meaning that the 6th column is correctly interpreted
as 6. Strand).
However, upon running "Fetch sequences" , Ex
files with different names in the
chromosome column?
Thanks a lot in advance,
Sarah
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Hi Hersh,
you can find a working wrapper for macs 1.4. when you follow the link in
the comments there:
https://bitbucket.org/galaxy/galaxy-central/issue/573/enable-macs-v14
Best regards,
Sarah
On 07/07/2011 10:19 AM, Hersh wrote:
Hi,
Has anyone tried configuring latest version of macs
and get the same problem
occurring each time.
Could you please help me find a fix for this?
Cheers,
Sarah
Traceback (most recent call last):
File "/Users/allabyrg/Desktop/galaxy-dist/tools/rgenetics/rgFastQC.py", line
141, in
assert os.path.isfile(opts.executable),'##rg
ah.ma...@inra.toulouse.fr) is a mistake. Could you
please delete the second one ?
Thank you in advance,
Sarah MAMAN
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Sarah Maman
INRA - LGC - SIGENAE
Chemin de Borde-Rouge - Auzeville - BP 52627
31326 Castanet-Tolosan cedex - FRANCE
Tel: +33(0)5.61.28.57.08
Tax: +33(0)5.61.28.
Dear,
I would like to protect Galaxy installed on my own server , with an
.htaccess file.
Unfortunalty, my .htaccess file seems not to be read. Only
universe_wsgi.ini seems to be read.
How can I modify universe_wsgi.ini to add an .htaccess ?
Thanks in advance,
Sarah MAMAN
ilog : job finished at ven avr 6 14:04:13 CEST 2012
Could you please help me ?
Thanks in advance,
Sarah Maman
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:
BWA run on single-end
An error occurred running this job: entree dans bwa for illumina
BWA Version: 0.6.1-r104
BWA run on single-end dataEpilog : job finished at ven avr 6 14:16:01
CEST 2012
entree dans bwa wapper
Thanks in advance,
Sarah Maman
Sarah Maman a écrit :
Hi Nate,
When I operate
ys.stderr.write('entree dans bwa wapper')" in comment to avoid
to display SAM file in red.
Faithfully,
Sarah Maman
Sarah Maman a écrit :
Hi,
This problem bellow is solved thanks to an eccho on $PATH and
$DRMAA_LIBRARY_PATH.
I have modified ~/.bash_profile file to define these
out that problem, so I'm also waiting on details on that
question, but for now, I'd just like to know what to make of the
output...
best,
Sarah
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n, that I should NOT identify my representative
sequence file to updated GI numbers using another pipeline, and then
bring the file of GI numbers to Galaxy to fetch taxonomic assignments?
(which I would do because of the nice neat columns for each taxonomic
level Galaxy puts out)
Sarah
On Mon, Apr
s the correct match is the listed GI value minus 1
(ie, in NCBI, gi|324034994 is not 527nt long, but 324034993 IS 527nt
long).
On Mon, Apr 23, 2012 at 11:05 AM, Peter Cock wrote:
> On Mon, Apr 23, 2012 at 5:56 PM, Sarah Hicks wrote:
>> I am having trouble finding information on the Me
on't know which
to pick. Is this problem well understood, yet?
On Tue, Apr 24, 2012 at 10:52 AM, Peter Cock wrote:
> On Mon, Apr 23, 2012 at 11:41 PM, Sarah Hicks wrote:
>> Peter, you requested an example, here are the first five hits for my
>> first query sequence (OTU#0)
>&g
Thanks for the update! I am not in a huge rush, but I was worried I
had not been describing the problem clearly, as it took quite a while
to explain to colleagues here :)
best
On Tue, Apr 24, 2012 at 3:24 PM, Jennifer Jackson wrote:
> Hi Sarah,
>
> We appreciate all of the information
Ok, I'll work on installing this...
On Tue, Apr 24, 2012 at 4:08 PM, Jennifer Jackson wrote:
> Thanks Peter,
>
> Excellent point. From there, the "Cut" tool could be used to reorganize the
> output to exactly match that of the 13-column regular megablast output. So,
> no external data needed, no
e any solution to drop these datasets in "saved datasets" ?
Thanks in advance,
Sarah Maman
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-0500
summary: Fix for populating the tool panel and generating the
integrated_tool_panel.xml file.
This behavior is not reproduce on your public server.
Thanks,
Sarah Maman
Jeremy Goecks a écrit :
Sarah,
I can't reproduce this behavior on a local instance or on our public server.
Dear All,
I was wondering if it would be possible to add Mycobacterium
tuberculosis H37Rv as a reference genome to the list of built-in indexes
in the Map with Bowtie for Illumina (version 1.1.2) tool.
Thank you,
Sarah
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Thanks Jen!
That solved my problem.
Sarah
On 8/22/2012 10:59 AM, Jennifer Jackson wrote:
Hello Sarah,
We can add this genome to the list to be indexed for Bowtie.
Meanwhile, quickest way to work with small genomes immediately is as a
custom genome. Simply load the genome into your history in
Hello,
I would like to know how to share a single dataset without sharing my
history through a local instance of Galaxy (with a LDAP identification) ?
Thanks in advance,
Sarah maman
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tilib] use_chiphorde4.rb started, usage
LLIB 08 Jan 09:10:17 [ytilib] run_chiphorde4.rb
Thanks in advance,
Sarah
Support a écrit :
Bonjour,
Voilà ce que j'obtiens quand je lance la commande qu'il demande:
ruby run_chiphorde4.rb
LLIB 08 Jan 09:10:17 [ytilib] ytilib required, working
Thanks to Marie-Stephane to have found that this error is due to a
diifference of verion.
Alban, could you please tell us which version (2 or 3) do you use in
your Galaxy tools, in order to install this version on our cluster ?
Thanks in advance,
Sarah
Sarah Maman a écrit :
Thanks Alban for
eur de syntaxe
près du symbole inattendu « ;; »
/work/galaxy/database/pbs/galaxy_4134.sh: line 13: `RepeatMasker
-parallel 8 -speci/
Do you have any ideas ?
Thank you in advance for your help,
Sarah Maman
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Sarah Maman
INRA - LGC - SIGENAE
http://www.sigenae.org/
Chemin de
ou dossier de ce type
cp: impossible d'évaluer « /work/tmp/tmpga_QOo/dataset_5979.dat.masked »: Aucun
fichier ou dossier de ce type
tail: impossible d'ouvrir « /work/tmp/tmpga_QOo/dataset_5979.dat.out » en
lecture: Aucun fichier ou dossier de ce type
Do you have any idea ?
Thanks i
me treatment won't run by lake of memory ..
If you have any idea on how to add option on Galaxy qsub, could you please help
me ?
I would like to add these options to qsub : qsub -l mem=6G -l h_vmem=8G
* _*ChIPMunk*_ :Sorry, but all ChIPMunk files (xml, pl; sh) didn't have execution
Thanks a lot Alban for these explanations ,
Everything is OK.
++,
Sarah
alermine a écrit :
Hi all,
* _*For the tool FilterControl*_, our cluster is configured to kill jobs that
use more than 4Go of memory.
I don't achieve to modify qsub options in my Galaxy instance, so I'he ch
tput.pl
script). Do you have any idea ?
Thanks in advance,
Sarah
Here is your last message :
- Here is the error I get when running the tool ChIPmunk (thanks Alban
for you help (ChIPMunk v2 is used and all librairies are found) but
here is a new error, maybe a problem of "dirname
alaxy
Event Horizon"?
Sincerely,
Sarah Maman
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Sarah Maman
INRA - LGC - SIGENAE
http://www.sigenae.org/
Chemin de Borde-Rouge - Auzeville - BP 52627
31326 Castanet-Tolosan cedex - FRANCE
Tel: +33(0)5.61.28.57.08
Fax: +33(0)5.6
Hello,
My question is about sharing histories _with a specific user._
The share is not effective for a specific one but for all users logged
in our local instance.
Could you please help me ?
Thank you in advance,
Sarah
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Sarah Maman
INRA - LGC - SIGENAE
http
Hello Jennifer,
I would like to share only with a specific user but when I use the meth
3 with the email address into last section, my history is not shared.
I need to publish AND share with a mail , in order to see my history in
shared data .
It seems to be a bug ?
Thanks in advance,
Sarah
Jennifer,
I agree with you : it's work in the public Main Galaxy instance but it
doesn't in my local instance of galaxy.
Maybe a problem of version ?
Would you like to test in my local instance ?
Thanks in advance,
Sarah
Jennifer Jackson a écrit :
Hi Sarah,
I am unable to dupl
Thanks a lot, it's OK now ;-)
Sarah
James Taylor a écrit :
Sarah, when you share with a specfic user, it will not show up under
the "Shared Data" section since that is only for published items. The
person you share it with should see it under "Histories Shared with
line? Please advise, at your earliest convenience-- I have a room full of
impatient newbie hackers ;)
Thank you!
--Sarah
Sarah Schaack, PhD
*Assistant Professor, Reed College*
*Fulbright Scholar, Centre for Bioinformatics and Biotechnology, University
% input_dbkey )
+chrom_info = os.path.join( trans.app.config.len_file_path,
"%s.len" % input_dbkey )
But I always have the same error message.
Could you please help us ?
Thanks in advance,
Sarah
//
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Sarah Maman
INRA - GenPhySE - SIGENAE
http://www.sigenae.org/
Chemin de Bo
add annotations to the already completed analysis would be terrific.
Thanks!
Sarah
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