Re: [galaxy-user] Cistrome

2011-10-26 Thread Jennifer Jackson

Hello Albena,

The Cistrome team should be contacted directly at:

   http://cistrome.org/
   cistrome-b...@jimmy.harvard.edu

Thanks,

Jen
Galaxy team

On 10/25/11 5:08 PM, Albena Pramatarova, Dr wrote:

Hi
What is the procedure for getting a username and password key to use the Aspera 
tool?
Thank you for your help.

Albena
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Re: [galaxy-user] Over disk quota

2011-10-26 Thread Nate Coraor
GANDRILLON OLIVIER wrote:
 Hello
 
 I just received the following message while using Galaxy through the web
 
 You are over your disk quota. Tool execution is on hold until your disk 
 usage drops below your allocated quota.
 
 I deleted a couple of files but it didn't helped.
 I checked the FAQ and could not get the answer.

Hi Olivier,

The FAQ page is out of date and we'll be updating this as soon as
possible.  Please see the following for information about how to free up
disk space:

http://wiki.g2.bx.psu.edu/Main
http://wiki.g2.bx.psu.edu/Learn/Managing%20Datasets

Sorry for the inconvenience, and thanks for using Galaxy.

--nate

 
 Thank's for your help
 
 Olivier
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Re: [galaxy-user] Names for genes in RNA-Seq analysis

2011-10-26 Thread GANDRILLON OLIVIER
Dear Carl

After having solved a couple of other problems, I am now to the point
where I can:
1.either get the FKPM and no names or
2. have the names and FKPM values to zero (or OK ?)

So I was wondering whether you had solved this FKPM value problem with
chicken you had?


Best

Olivier


Le 26/10/11 02:21, « Jennifer Jackson » j...@bx.psu.edu a écrit :

Hello Carl,

Your question is similar to Olivier's, even though the problem is
presenting in a different way. There is most likely a data mismatch
problem as explained in my earlier reply to this thread and this prior
mailing list question:
http://gmod.827538.n3.nabble.com/Cufflinks-reporting-FPKM-values-of-all-ze
roes-0-tt3183517.html#a3183928

Best wishes for your project as well,

Jen
Galaxy team

On 10/20/11 7:32 AM, Carl Schmidt wrote:
 I am also using Galaxy to analyze RNA-seq libraries from chicken.
 While the names of the genes appear in the Cufflinks output, the FPKM
 values are all zero.


 On Oct 20, 2011, at 9:12 AM, GANDRILLON OLIVIER wrote:

 Hello

 I am using Galaxy to analyse RNA-seq libraries made from chicken cells.

 I just groomed my sequences, passed them through TopHat and then
 Cufflinks.

 This worked well and in the end I get a list of genes and their
 respective FPKM values.

 My only problem is that the names of the genes do not appears in the
 listing, they are simply reference as CUFF.1, CUFF.2,  etcŠ

 Could you please tell me how I could obtain gene names? (I went
 through the FAQ and could not get the answer).

 Sincerely

 Olivier



 -
 New mail adress: olivier.gandril...@univ-lyon1.fr
 mailto:olivier.gandril...@univ-lyon1.fr

 Dr Olivier Gandrillon
 Centre de Génétique et de Physiologie Moléculaires et Cellulaires
 UMR CNRS 5534
 Université Claude Bernard Lyon I
 Bat Gregor Mendel (ex 741)
 16, rue Raphaël Dubois
 69622 Villeurbanne Cedex
 Phone : 04-72-44-81-90
 Fax : 04-72-43-26-85
 Web adress :
 Lab: http://cgphimc.univ-lyon1.fr/spip.php?rubrique33lang=en
 http://cgphimc.univ-lyon1.fr/spip.php?rubrique33lang=en
 Perso: http://www.cgmc.univ-lyon1.fr/Gandrillon/OG/OG1.html

 Comment obtenait-il l'adhésion du peuple aux nouveaux mensonges qu'il
 inventait chaque jour? Précisément parce que c'était des mensonges et
 précisément parce qu'ils étaient une insulte à la perception. Le
 peuple était hypnotisé par l'aplomb, ce droit qu'il s'octroyait de
 contredire l'évidence. Les gens portaient un regard médusé sur un
 Goebbels déchaîné. Ils voyaient en transparence son souhait énorme de
 nier le nain boiteux

 Tobie Nathan, in Qui a tué Arlozoroff

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 Carl Schmidt
 Associate Professor
 Animal  Food Sciences
 University of Delaware
 Newark, DE 19716
 051 Townsend Hall
 schmi...@udel.edu mailto:schmi...@udel.edu
 302-831-1334








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-- 
Jennifer Jackson
http://usegalaxy.org
http://galaxyproject.org/wiki/Support


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Re: [galaxy-user] Names for genes in RNA-Seq analysis

2011-10-26 Thread Michael Gooch
Regarding the GTF files for cuffllinks, how do I obtain one for all 
human mRNA that actualy contains gene names rather than accession 
numbers. I went to the UCSC table browser but their files contain 
accession numbers that I dont know how to decode en-masse.

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Re: [galaxy-user] permanently delete problem

2011-10-26 Thread Nate Coraor
Richard Mark White wrote:
 hi,
   so i went to options--saved history--advanced--deleted datasets.  then 
 checked all of them, and then hit permanently delete.
 but nothign happened.  they still show up as deleted, and they are taking up 
 lots of my quota.
 how do i get rid of these?
 
 rich

Hi Rich,

I'm not sure what's going on here, I'm looking in to it.

--nate
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Re: [galaxy-user] permanently delete problem

2011-10-26 Thread Richard Mark White
actually, i just waited a bit and now they are deletd.
r





From: Nate Coraor n...@bx.psu.edu
To: Richard Mark White whit...@yahoo.com
Cc: GANDRILLON OLIVIER olivier.gandril...@univ-lyon1.fr; 
galaxy-u...@bx.psu.edu galaxy-u...@bx.psu.edu
Sent: Wednesday, October 26, 2011 12:55 PM
Subject: Re: permanently delete problem

Richard Mark White wrote:
 hi,
   so i went to options--saved history--advanced--deleted datasets.  then 
 checked all of them, and then hit permanently delete.
 but nothign happened.  they still show up as deleted, and they are taking up 
 lots of my quota.
 how do i get rid of these?
 
 rich

Hi Rich,

I'm not sure what's going on here, I'm looking in to it.

--nate___
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[galaxy-user] sample for video for example 3 in ngs analyses in galaxy

2011-10-26 Thread Linda McMahan
Hi,

I am watching the video 'Example
3http://screencast.g2.bx.psu.edu/galaxy/quickie12_illumina_pe/flow.html
-
mapping paired-end Illumina run and visualizing results at UCSC Browser', and
would like to try out the exercise.  I don't have paired-end Illumina
fastq sample, Could you provide me the sample mentioned in the video or
point me to the location where I can get a small human paired-end Illumina
fastq sample to try out the exercise in example 3.

Thanks,
Linda McMahan
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Re: [galaxy-user] permanently delete problem

2011-10-26 Thread Nate Coraor
Great, thanks for letting us know.

Richard Mark White wrote:
 actually, i just waited a bit and now they are deletd.
 r
 
 
 
 
 
 From: Nate Coraor n...@bx.psu.edu
 To: Richard Mark White whit...@yahoo.com
 Cc: GANDRILLON OLIVIER olivier.gandril...@univ-lyon1.fr; 
 galaxy-u...@bx.psu.edu galaxy-u...@bx.psu.edu
 Sent: Wednesday, October 26, 2011 12:55 PM
 Subject: Re: permanently delete problem
 
 Richard Mark White wrote:
  hi,
    so i went to options--saved history--advanced--deleted datasets.  then 
  checked all of them, and then hit permanently delete.
  but nothign happened.  they still show up as deleted, and they are taking 
  up lots of my quota.
  how do i get rid of these?
  
  rich
 
 Hi Rich,
 
 I'm not sure what's going on here, I'm looking in to it.
 
 --nate
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[galaxy-user] Genome database/builds missing?

2011-10-26 Thread Daniel N. Hupalo
I've been using galaxy to analyze maf files and today the drop down list for 
database/builds for genomes has lost most of the genomes once listed. 

I no longer see any bacteria or plants on the list, specifically TAIR9 
arabidopsis is no longer on the drop down list when it was just yesterday. Did 
something change? 

Thanks

- Dan

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[galaxy-user] cluster install

2011-10-26 Thread Joshua Udall
Dear Galaxy -

We would like to install and instance of Galaxy on our campus cluster.
 The install process looks very straight forward, but tying it in with
our authentication system for the current, functioning cluster may not
be as simple.  It appears that galaxy is easy to install if there are
limited users on a local machine or on a cluster where galaxy is the
main use of the cluster (so it handles all the user accounts).  Where
would I direct our IT admin group to get more assistance with
customizing the authentication process with our existing, function
cluster?

-- 
Joshua Udall
Assistant Professor
295 WIDB
Plant and Wildlife Science Dept.
Brigham Young University
Provo, UT 84602
801-422-9307
Fax: 801-422-0008
USA
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[galaxy-user] cluster install

2011-10-26 Thread Joshua Udall
Dear Galaxy -


We would like to install and instance of Galaxy on our campus cluster.

 The install process looks very straight forward, but tying it in with

our authentication system for the current, functioning cluster may not

be as simple.  It appears that galaxy is easy to install if there are

limited users on a local machine or on a cluster where galaxy is the

main use of the cluster (so it handles all the user accounts).  Where

would I direct our IT admin group to get more assistance with

customizing the authentication process with our existing, function

cluster?


--

Joshua Udall

Assistant Professor

295 WIDB

Plant and Wildlife Science Dept.

Brigham Young University

Provo, UT 84602

801-422-9307tel:801-422-9307

Fax: 801-422-0008tel:801-422-0008

USA
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Re: [galaxy-user] cluster install

2011-10-26 Thread Oleksandr Moskalenko
It's reasonably easy to set up Galaxy to use external authentication. We 
modeled our authentication after the way MSI folks did it as posted on the 
galaxy-dev list a while ago. We use SSO (Single Sign On) with mod_auth_tkt SSO 
tied into an LDAP back-end used for our cluster. I'd be happy to share the 
details beyond the LDAP authentication discussion you can find in the Galaxy 
list archives [1] if necessary. In addition, this sort of question is more 
appropriate to the galaxy-dev, but not the galaxy-user list.

Regards,

Alex

--
Oleksandr Moskalenko, Ph.D.
Biological Applications Support
High Performance Computing Center
University of Florida

1. http://lists.bx.psu.edu/pipermail/galaxy-dev/2010-May/002660.html
http://lists.bx.psu.edu/pipermail/galaxy-dev/2010-May/002667.html

On Oct 26, 2011, at 12:29 PM, Joshua Udall wrote:

 Dear Galaxy -
 
 
 
 We would like to install and instance of Galaxy on our campus cluster.
 
  The install process looks very straight forward, but tying it in with
 
 our authentication system for the current, functioning cluster may not
 
 be as simple.  It appears that galaxy is easy to install if there are
 
 limited users on a local machine or on a cluster where galaxy is the
 
 main use of the cluster (so it handles all the user accounts).  Where
 
 would I direct our IT admin group to get more assistance with
 
 customizing the authentication process with our existing, function
 
 cluster?
 
 
 
 --
 
 Joshua Udall
 
 Assistant Professor
 
 295 WIDB
 
 Plant and Wildlife Science Dept.
 
 Brigham Young University
 
 Provo, UT 84602
 
 801-422-9307
 
 Fax: 801-422-0008
 
 USA
 
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[galaxy-user] Problem with bam and/or bai files

2011-10-26 Thread Mike Dufault
Hello Galaxy Team,
 
I have been using Galaxy for SNP detection for with great success. Basically, I 
followed the screen-cast from Anton without any problems. The only change was 
to use the BWA instead of Bowtie. Until now, I have always assigned my raw read 
files to the hg19 format. Now I want to try the GATK pipeline to analyze my 
samples but I am running into a problem with the bam/bai files.
 
Here is what I did. I imported my Illumina paired end reads into Galaxy and 
assigned them to the hg_g1k_v37 format instead of the Hg19 format. From there, 
I again followed the exact same process: FastQ Groomer, Summary Statistics, 
Boxplots, Align with BWA, filter on SAM, SAM-to-Bam, generate bai file. I made 
sure that hg_g1k_37 was chosen for the format for all of these steps that 
required that information.
 
Everything seemed to run successfully as all of the boxed turned green. When I 
tried to view the bam file in IGV (as a QC step before the GATK pipeline), I 
received the following error: Error reading bam file. This usually indicates a 
problem with the index (bai) file. ArrayIndexOutofBoundsException: 4682 (4682).
 
I did the exact same analysis using the Hg19 format and my bam/bai files worked 
perfectly fine in the IGV viewer. Can anyone tell me what the problem is and 
how to fix it?
 
Thanks,
Mike Dufault
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Re: [galaxy-user] Problem with bam and/or bai files

2011-10-26 Thread Jim Robinson

 Hi Mike,

Someone from the Galaxy team can perhaps give some insight on what went 
wrong,  I can comment on the error message from IGV.   That error is 
thrown from Picard, in every case I've investigated so far it was traced 
to a problem with the index.  The most common causes are (1) a problem 
with the sequence dictionary in the BAM header itself, specifically 
incorrect sequence lengths, and (2) indexing an un-sorted BAM.  
Apparently samtools will make invalid indexes from such files without 
any complaints in both cases.  You can even use samtools tview on such 
files,  it happily will show you some random region when you query.


I don't see a Sort step in your workflow, maybe that's the problem?

Please CC me on any reply,  I might miss it in the list.

Jim




Hello Galaxy Team,
I have been using Galaxy for SNP detection for with great success. 
Basically, I followed the screen-cast from Anton without any problems. 
The only change was to use the BWA instead of Bowtie. Until now, I 
have always assigned my raw read files to the hg19 format. Now I want 
to try the GATK pipeline to analyze my samples but I am running into a 
problem with the bam/bai files.
Here is what I did. I imported my Illumina paired end reads into 
Galaxy and assigned them to the hg_g1k_v37 format instead of the Hg19 
format. From there, I again followed the exact same process: FastQ 
Groomer, Summary Statistics, Boxplots, Align with BWA, filter on SAM, 
SAM-to-Bam, generate bai file. I made sure that hg_g1k_37 was chosen 
for the format for all of these steps that required that information.
Everything seemed to run successfully as all of the boxed turned 
green. When I tried to view the bam file in IGV (as a QC step before 
the GATK pipeline), I received the following error: Error reading bam 
file. This usually indicates a problem with the index (bai) file. 
ArrayIndexOutofBoundsException: 4682 (4682).
I did the exact same analysis using the Hg19 format and my bam/bai 
files worked perfectly fine in the IGV viewer. Can anyone tell me what 
the problem is and how to fix it?

Thanks,
Mike Dufault


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