Hi Dao,
To run the analysis correctly on SOLiD data, a local or cloud Galaxy
would be needed. A cloud Galaxy is web based and if you follow the links
below, you will find exact instructions for getting set up. There are
Amazon fees, but they do have various grant programs that you can review
at their site for help with that. Galaxy itself is always free!!
About tools on the Test server .. these are constantly in flux in terms
of dependencies and such, and we don't support them because this is
truly a development environment for us. You may find that certain tools,
including this one, work on smaller datasets at some point in the
future, but for the public this shouldn't be used for serious work.
One last option, and I don't know for certain if there is one in here
that will accept your datatype and enough quota to do significant work
(these also change over time), are other public Galaxy servers. Each is
supported by the hosting group. A list is here and you can look
through/review the sites to see what is available:
http://wiki.galaxyproject.org/PublicGalaxyServers
Take care,
Jen
Galaxy team
On 11/26/13 7:43 AM, Ly, Dao wrote:
>
> Hi
>
> Thank you very much for your reply. For the time being, I just wanted
> to be familiarized with the workflow and the open resource of galaxy
> main to analyze NGS. If you could advise me how I can obtain the RPKM
> that will be great. I have tried many ways to map but no luck so far.
> I think I’m at the end of my wits.
>
> I did try tophat2 with ion torrent data and it worked fine. This solid
> SRA format is giving me a hard time and I can only work on webbase
> program. I also try tophat for solid on test server but it failed!
> Many thanks again
>
> Best regards
>
> Dao
>
> *From:*Jennifer Jackson [mailto:j...@bx.psu.edu]
> *Sent:* November 20, 2013 8:46 PM
> *To:* Ly, Dao; galaxy-user@lists.bx.psu.edu
> *Subject:* Re: [galaxy-user] Cufflinks returned 0 value in all RPKMs
>
> Hello,
>
> If the data is RNA from rat, then you will want to be using Tophat
> instead of Bowtie. Otherwise the data will not be mapped as spliced
> the results will be off in many ways (the fragments counts are a small
> symptom of a larger problem).
>
> You can use 'Tophat for SOLiD' on a suitable local or cloud Galaxy
> instance. It is available on the Test server, but tools are not
> supported here (we test/break things!) and the quotas are just 10G
> with an account. But maybe is a place to do a small trial run before
> committing to a cloud server.
> http://getgalaxy.org
> http://usegalaxy.org/cloud
> http://usegalaxy.org/toolshed
>
> More about RNA-seq is in our wiki and public server, including
> link-outs and tutorials, you can get started here:
> Example → RNA-seq analysis tools:
> http://wiki.galaxyproject.org/Support#Interpreting_scientific_results
> See RNA-seq examples: http://wiki.galaxyproject.org/Learn#Other_Tutorials
>
> Best,
>
> Jen
> Galaxy team
>
> On 11/20/13 6:09 AM, Ly, Dao wrote:
>
> Hi
>
> I have been trying to analyze a rat Solid SRA but I encountered a
> problem: cufflinks gave me 0 RPKM in all genes. Here is my workflow
>
> 1.Get data with EBI SRA: sent the fastaq file directly to galaxy
>
> 2.Fastaq groomer
>
> 3.Mapped with bowtie for Solid (paire-ended) with the built- in
> index rat rn5 as reference genome
>
> 4.Sam to Bam the bowtie mapping result
>
> 5.Cufflinks the bam file
>
> All RPKMs of gene expression and transcript expression have a 0
> value even thought the RPKM status is OK. I used default setting
> for all jobs. Am I missing something? Any help, suggestion will be
> greatly appreciated. Thank you very much
>
> Best regards
>
> Dao
>
>
>
>
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> --
> Jennifer Hillman-Jackson
> http://galaxyproject.o
