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4 Apr
2010
4 Apr
'10
9:32 p.m.
Hi list, Is there a tool in Galaxy to trim the end of FASTQ reads based on their quality, say to remove all base pairs at the end of a read that have a quality smaller than 20? I know about the tool that trims an arbitrary number of base pairs at the end of reads and the filter tool that can filter out sequences that have some base pairs with a quality value below some threshold but they are different from what I need. Regards, Florent