Hi Bin,

The reply given for this same question posted at seqanswers is correct, including the Tool Shed comments:
http://seqanswers.com/forums/showthread.php?t=14106

To give a bit more detail, when using the public Galaxy instance at http://usegalaxy.org, the idea would be to run the "NGS: QC and manipulation -> Clip" tool with each adapter, one at a time. Each time start with the same original file and only output sequences that are clipped. Then merge at the end, if wanted, for downstream analysis.

The Clip tool is sourced from the FASTX-toolkit and currently does only work for 3' adapters. You may want to contact the tool author Assaf Gordon if you have a suggestions/use cases for tool enhancements http://hannonlab.cshl.edu/fastx_toolkit/.

Just so you know, there are tools that simply trim off bases, from either end, which may or may not work for needs. Please see "FASTQ Trimmer" and "Trim sequences".

I also opened a bitbucket ticket to track the ideas for expanding the options for this type of function. This can be tracked at:
http://bitbucket.org/galaxy/galaxy-central/issue/659/expand-adapter-sequence-clipping-options

Hopefully one of the available options will work out for your project,

Best,

Jen
Galaxy team


On 9/14/11 2:17 PM, Binbin You wrote:
Hi All,

In " Clip adapter sequences" option of Penn State Galaxy, I choose
"Enter custom sequence" under "Source", and I can only enter One custom
clipping sequence. So how can I enter another 3 adapter sequences which
I want to clip.

In addition, In "*What it does" it shows: *
This tool clips adapters from the 3'-end of the sequences in a
FASTA/FASTQ file.

So how could i do if I have the adapter sequences like this:

5' TACACTCTTTCCCTACACGACGCTCTTCCGATCT
5 'AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTA
5' GACGGCATACGAGCTCTTCCGATCT
5' AGATCGGAAGAGCTCGTATGCCGTC

Thanks very much for any response!

Best wishes,
Bin


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