Hello,

This Galaxy wrapper is based on the FASTX-Toolkit tool by the same name. A link to the original is at the bottom of the tool's form in the UI. To see the Galaxy wrapper, it is in the source here: galaxy-central / tools / fastx_toolkit
https://bitbucket.org/galaxy/galaxy-central

Questions about the core tool can be directed to the tool author. Help with running a local Galaxy or tools in general is on the galaxy-dev@bx.psu.edu mailing list: http://wiki.galaxyproject.org/Support#Mailing_Lists

If you create a new wrapper with more options, please consider contributing it to the Tool Shed, as this tool is super popular and the option for 5' clipping has come up before. http://wiki.galaxyproject.org/Tool%20Shed

Take care,

Jen
Galaxy team


On 8/22/13 12:58 PM, William Yarosh wrote:
Thanks,

I'm trying to figure out how to use these programs.

Do you know where I can get the source code for clip?  I think I can edit the program to look at the 5' end if I see it.

Will

On Aug 22, 2013, at 3:19 PM, Jennifer Jackson <jen@bx.psu.edu> wrote:

Hello,

The "Clip" program only acts on the 3' end. In some cases, running "FastQC" to isolate adapter regions, then using a tool like "FASTQ Trimmer" or "Trim" will work (if the lengths are somewhat fixed).

Alternately, the tools "NGS: QC and manipulation -> Reverse-Complement or Manipulate FASTQ" will reverse compliment reads. For the second, the option is located in Manipulate Reads -> Manipulate on 'Sequence Content' -> Sequence Manipulation Type:. There are several options here, including trim again, but also "Reverse Complement".

Hopefully this helps!

Jen
Galaxy team


On 8/22/13 12:03 PM, William Yarosh wrote:
Hi,

I was using the clip program, but my adapters are on the 5' end.  Is there any way to use this program so it will clip the 5' end or a way to make all my reads the reverse complement and run it through this program?

Thanks
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Jennifer Hillman-Jackson
http://galaxyproject.org