On Tue, Oct 16, 2012 at 8:22 PM, Fang,Xiefan <xiefanf...@ufl.edu> wrote:
> Dear Galaxy users,
>          Does anyone know how to merge several FASTQ groomer files by using
> Galaxy? If not, is there any other program that can achieve this?  The size
> of one FASTQ groomer file is around 1GB. Thank you!

The Galaxy tool "Concatenate datasets tail-to-head" under "Text Manipulation"
should work. I'm assuming you just need a simple concatenation of individual
FASTQ files, not a more complex merge dealing with duplicates or sorting.

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