Does Ray work with fasta input files?  More specifically, would it work 
with a "fastq" file that was really in fasta format (missing the quality 
value lines?)  I'm asking because I'm running khmer digital 
normalization http://khmer.readthedocs.org/en/latest/introduction.html 
on an Illumina HiSeq2000 data set, and the strip-and-split-for-assembly 
script in the khmer package strips out quality info when it is 
separating paired reads from singles.

Thank you,
Susan Miller
ARL BioComputing


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