Hi,
I just notice that NGS FASTQ
Trimmer<https://usegalaxy.org/tool_runner?tool_id=toolshed.g2.bx.psu.edu%2Frepos%2Fdevteam%2Ffastq_trimmer%2Ffastq_trimmer%2F1.0.0>by
column can't detect the fastq file I loaded. Anyone knows why. thanks
a
lot.


On Fri, Jan 24, 2014 at 11:00 AM, <galaxy-user-requ...@lists.bx.psu.edu>wrote:

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> Today's Topics:
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>    1. Re: Creating a Trackster visualisation from a     reference in
>       your history (Jeremy Goecks)
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> ----------------------------------------------------------------------
>
> Message: 1
> Date: Thu, 23 Jan 2014 15:49:44 -0500
> From: Jeremy Goecks <jgoe...@email.gwu.edu>
> To: graham etherington (TSL)
>         <graham.ethering...@sainsbury-laboratory.ac.uk>
> Cc: galaxy-user@lists.bx.psu.edu
> Subject: Re: [galaxy-user] Creating a Trackster visualisation from a
>         reference in your history
> Message-ID: <c3382f38-d243-4979-b6a7-ba13ef161...@email.gwu.edu>
> Content-Type: text/plain; charset="windows-1252"
>
> > Is it possible to create a custom build and use it to view a SAM file
> without adding the .len and .2bit files in to the Galaxy file system as an
> administrator?
>
> Yes, it definitely is.
>
> > If so, what am I doing wrong?
>
>
> This is a Galaxy bug which has been fixed in this commit:
>
>
> https://bitbucket.org/galaxy/galaxy-central/commits/117fef56513fc563dd231516196cfd601c1635e2
>
> We have a release coming up, so this fix will be included in the release
> and will make it to our public server soon. In the meantime, note that you
> can use the genome fasta file rather than the len file to create a custom
> build and everything should work.
>
> Thanks,
> J.
>
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-- 
Gang Wang
Ph.D. student
Veterinary Integrative Bioscience
College of Veterinary Medicine & Biomedical Sciences
Texas A&M University
College Station, TX  77843-4458
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