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Question: How To Merge Fastq Groomer Files In Galaxy?
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gravatar for Fang,Xiefan
6.1 years ago by
Fang,Xiefan • 30
United States
Fang,Xiefan • 30 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! Best regards, Xiefan Fang, Ph.D. Postdoctoral associate Department of Pediatrics College of Medicine University of Florida Phone: 352-294-5675 Email: xiefanfang@ufl.edu
galaxy • 1.7k views
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modified 6.1 years ago by Peter Cock • 1.4k • written 6.1 years ago by Fang,Xiefan • 30
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gravatar for Peter Cock
6.1 years ago by
Peter Cock • 1.4k
European Union
Peter Cock • 1.4k wrote:
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
ADD COMMENT • link written 6.1 years ago by Peter Cock • 1.4k
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