[galaxy-user] mount issue

2012-05-08 Thread Zeeshan Ali Shah
HI, I am getting this when start cluster first time .
Error mounting file system '/mnt/galaxyData' from '/dev/sdg3', running
command '/bin/mount /dev/sdg3 /mnt/galaxyData' returned code '32' and
following stderr: 'mount: you must specify the filesystem type '

Is this a bug ? shd i avoid ..


BR

Zeeshan
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[galaxy-user] /mnt/galaxyIndices/hg19/bwa/base/hg19 not found

2012-05-08 Thread Zeeshan Ali Shah
Hi, I was following screenshot and after adding workflow
http://s3.amazonaws.com/heteroplasmy/heteroplasmy_information.html

Upon running it is mentioning that /mnt/galaxyIndices/hg19/bwa/base/hg19
which does not exist .. i have confirmed that after login to instance
directly.

due to this reason it is unable to pick FASTQ file.
any hint ?

Also. When we newly create cloud man from AMI dated 22nd March 2011, Does
it make sense to update Galxy via admin ? or just run it with out update..

BR

Zeeshan
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Re: [galaxy-user] Help on installing cutadapt

2012-05-08 Thread Jennifer Jackson

Hello Tilahun,

Are you logged into your Galaxy instance UI using your admin account? 
This will display the Admin menu.


Admin permissions are set up in the universe_wsgi.ini file:

# -- Users and Security

 other items 

# Administrative users - set this to a comma-separated list of valid Galaxy
# users (email addresses).  These users will have access to the Admin 
section

# of the server, and will have access to create users, groups, roles,
# libraries, and more.  For more information, see:
# http://wiki.g2.bx.psu.edu/Admin/Interface
#admin_users = None

Hopefully this solves the issue. Going forward, you'll probably find 
that the galaxy-...@bx.psu.edu mailing list is the most helpful for 
local install questions:

http://wiki.g2.bx.psu.edu/Support#Mailing_Lists

Best,

Jen
Galaxy team

On 5/8/12 2:10 PM, Tilahun Abebe wrote:

Hi Galaxy users,

I tried to install cutadapt for sequence trimming on a local Galaxy
instance. I successfully installed Galaxy as an administrator. However,
when Galaxy starts, I don't see the administrator option in the top menu
bar with the Analyze Data, Workflow, Shared Data, Visualization, Help,
and User. It looks like the only way I can install cutadapt is with an
administrator option. Any suggestion how I can include the administrator
option in the menu?

Thanks for your help.

Tilahun



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--
Jennifer Jackson
http://galaxyproject.org
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Re: [galaxy-user] operate on genomic intervals

2012-05-08 Thread Jennifer Jackson

Hi Jose,

That's great news! A tool tip in the wiki or UI would probably be 
helpful - your question was a good one. Meanwhile, I'll post your 
results to back to the list, it may help others who are also working to 
optimize.


Glad that it worked out so well,

Jen
Galaxy team

On 5/8/12 2:57 PM, Xianrong Wong wrote:

Thank you Jennifer!  I swapped the order of the input datasets which
reduced the running time from 2 hrs to 10 min!
Jose

On Mon, May 7, 2012 at 12:03 PM, Jennifer Jackson j...@bx.psu.edu
mailto:j...@bx.psu.edu wrote:

Hi Jose,

Very glad to know that you have this working.

You question is difficult to address with specificity, as these are
completely different algorithms. But in general, any alignment
algorithm (Bowtie included) has some sort of indexing strategy (some
are better than others) to minimize what is held in memory and
process bulk data through. See the Bowtie documentation for how this
is achieved.

The interval operations tools also have an indexing strategy,
specifically, the second input file is the portion loaded memory and
the first file is processed against it. So, if you want use an
extremely large dataset (or just want to the job to run quicker) try
to use it as the first input file if possible.

These tools are designed to be used together and with other tools to
create workflows, so there should pretty much always be some way to
break jobs up (as you did) to get them through the tools, on even
modest systems:
http://wiki.g2.bx.psu.edu/__Learn/Interval%20Operations
http://wiki.g2.bx.psu.edu/Learn/Interval%20Operations

Take care,

Jen
Galaxy team



On 5/7/12 8:30 AM, Xianrong Wong wrote:

Hello Jennifer,  thanks for the advise.  It worked when I did it a
chromosome at a time.  Is there a reason why this is so much more
computationally heavy as compared to bowtie?  (mapping 190
million reads
took only 3-4 hours for me)
Jose

On Fri, May 4, 2012 at 7:55 PM, Jennifer Jackson j...@bx.psu.edu
mailto:j...@bx.psu.edu
mailto:j...@bx.psu.edu mailto:j...@bx.psu.edu wrote:

Hello Jose,

It sounds as if the job is running out of memory. Since you are
already working on a cloud, I am going to make the
assumption that
you have explored the server options with high-capacity memory
there. But if not, that is one place to start, in particular
your
EC2 Instance type, as described on this wiki:
http://wiki.g2.bx.psu.edu/Admin/Cloud/CapacityPlanning
http://wiki.g2.bx.psu.edu/__Admin/Cloud/CapacityPlanning

http://wiki.g2.bx.psu.edu/__Admin/Cloud/CapacityPlanning
http://wiki.g2.bx.psu.edu/Admin/Cloud/CapacityPlanning

However, even if that was an option, you may want to consider
running your in data through in another way - by running smaller
jobs, then merging results, to avoid the large jobs. For
example, in
the last step where you join to the full BamHI delimited
bin file,
instead join to groups of bins in that file (perhaps grouped by
chromosome), then combine the results to produce the full
output.

Hopefully this helps provide some options,

Jen
Galaxy team


On 5/4/12 2:18 PM, Xianrong Wong wrote:

Hello,
 I have binned the mouse genome into fragments
based on
restriction enzyme cut sites.  So each bin is a fragment
flanked
by say
BamHI.  The output file is in the interval format: chr#
start
and end
coordinates of each bin.  I want to count how many times
each
bin has
reads that align to it.  I mapped my reads using bowtie and
generated a
dataset (interval format) for the aligned reads.  I then
used
join in
operate on genomic intervals and asked it to return intervals that
innerjoin the bin file.  The subsequent steps involve
grouping and
counting and then joining back to the 1st dataset (BamHI
delimited
bins).  I have tried this workflow on small datasets and
it worked.
However when I subject my full alignment file and full BamHI
delimited
bin file, the tool fails.  I am doing this on cloud.
  Any advice
would
be appreciated!

Jose



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