Can't seem to find an answer to this on your wiki site and it's not in
the tutorial.  I would like to filter my 454 reads for high quality
regions, rename the resulting sequence fragments AND relink the new
reads (fragments) to the original quality data so that I can take these
filtered reads and assembly them using MIRA. Is there a way to do this
with Galaxy?  So basically all I want to do is take the new read
fragments I get from converting the tabular file to the fasta file as
shown in your metagenomics tutorial, and generate a corresponding qual
file for these 'new' reads.


Best regards,



Aaron Jex, BSc, PhD

Senior Research Officer,

Department of Veterinary Science,

The University of Melbourne,

250 Princes Highway,

Werribee, Victoria,


tel: +61 3 9731 2294

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