Jeremy,

Usually, the users saved the files to their local machine by clicking on the 
links, and then uploaded them again to the galaxy server.
It can be possible to copy the link location, and paste it into the upload 
tools URL textarea.

Ideally, it would be nice for the tool developer to be able to include a link in the html 
that would "promote" the file to a dataset in the current history.

JJ

On 7/19/11 3:08 PM, Jeremy Coate wrote:
Thanks, Jim!

I'll see if my limited Galaxy/bioinformatics skills can rise to the challenge of using 
your wrapper (I've never visited the "tool shed" before).

Out of curiosity, how did people use the files generated by the barcode 
splitter without this? I'm assuming there was/is a way, but I'm not figuring it 
out.

Jeremy


On Tue, Jul 19, 2011 at 11:26 AM, Jim Johnson <johns...@umn.edu 
<mailto:johns...@umn.edu>> wrote:

        I've had users make a similar request for the split files to appear in their history. I made my own wrapper to enable this behavior. It presents 
a list of barcodes from the barcode file input. Any barcodes the user selects will have the resulting files copied to the users history as new datasets. 
I uploaded my barcode splitter tool configs to the toolshed: http://toolshed.g2.bx.psu.edu/ as repository: barcode_splitter JJ Date: Mon, 18 Jul 2011 
13:33:58 -0700 From: Jeremy Coate <je...@cornell.edu> <mailto:je...@cornell.edu> To: David K Crossman <dkcro...@uab.edu> 
<mailto:dkcro...@uab.edu> Cc: "galaxy-user@lists.bx.psu.edu" <mailto:galaxy-user@lists.bx.psu.edu> 
<galaxy-user@lists.bx.psu.edu> <mailto:galaxy-user@lists.bx.psu.edu> Subject: Re: [galaxy-user] using files produced by "Barcode 
Splitter" Message-ID: <caa2bwd5ueraqeoueq97tfnhkwvhziq89whvr-oy04ov-k4j...@mail.gmail.com> 
<mailto:caa2bwd5ueraqeoueq97tfnhkwvhziq89whvr-oy04ov-k4j...@mail.gmail.com> Content-Type:
        text/plain; charset="iso-8859-1" Thanks David, I had considered this possibility 
but, curiously, the files don't show up in the FastQ Groomer pull-down menu either. The original 
(multiplexed) data file that I split using the Barcode Splitter is there (and, incidentally, I ran 
FastQ Groomer on that before doing the barcode split), but none of the 3 files resulting from the 
splitter show up. Any other thoughts? It seems like the new files just aren't landing in my history, 
though I can look at them by clicking their links from the Barcode Splitter output. Jeremy On Mon, 
Jul 18, 2011 at 12:01 PM, David K Crossman <dkcro...@uab.edu> <mailto:dkcro...@uab.edu> 
wrote:

        Jeremy,**** ** ** The files need to be groomed using the FastQ Groomer so that they will 
end up in the fastqsanger state. Then your files will show up in the pull-down menus.**** ** ** 
David**** ** ** ** ** *From:* galaxy-user-boun...@lists.bx.psu.edu 
<mailto:galaxy-user-boun...@lists.bx.psu.edu> [mailto: galaxy-user-boun...@lists.bx.psu.edu 
<mailto:galaxy-user-boun...@lists.bx.psu.edu>] *On Behalf Of *Jeremy Coate *Sent:* Monday, 
July 18, 2011 1:44 PM *To:* galaxy-user@lists.bx.psu.edu 
<mailto:galaxy-user@lists.bx.psu.edu>

        *Subject:* [galaxy-user] using files produced by "Barcode Splitter"****

        ** **

        I used the "Barcode Splitter" tool to split multiplexed RNA-Seq 
libraries
        into separate files. I would now like to map the reads from each of 
these
        fastq files to a reference genome. However, the fastq files generated by
        Barcode Splitter don't appear in the "Fastq File" pull-down menus 
within the
        the BWA or Bowtie launch pages. I'm probably missing something obvious, 
but
        what is the trick for making these files available for the mapping 
tools? Do
        I need to import them into my history somehow?****

        ** **

        Thanks!
        Jeremy****






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