The tool "NGS: QC and manipulation -> FASTQ Groomer" will prepare your data and make it recognized by other formatting/analysis tools, including "Clip".

Please give this a try and let us know if you have any questions. For general help, please see http://galaxyproject.org/wiki/Learn


Galaxy team

On 11/14/11 11:04 AM, dtr...@ira.cinvestav.mx wrote:
Does anyone know if it is possible to trim sequencing adaptor sequences
away in Galaxy? and what is the necessary format for trimming sequences?
because  in Clip adapter sequences I can not to see my files.


Diana Trejo, PhD

Jennifer Jackson
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