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. Peter ___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list: http://lists.bx.psu.edu/listinfo/galaxy-dev To manage your subscriptions to this and other Galaxy lists, please use the interface at: http://lists.bx.psu.edu/
