Hello all, I have a 24GB RHEL5 machine on which I was able to do a de novo assembly of 454 paired-end and fragment reads (~1.5 million reads). I also have about 6 million 36bp Illumina reads. I would like to: 1) Map the Illumina reads to the 454 backbone 2) Include the Illumina reads with the 454 reads for a de novo assembly But I believe I don't have enough memory to handle all the Illumina reads. I think my VM could handle maybe 20% of the Illumina reads. What is the best way to reduce the Illumina reads used for the mapping and/or the de novo assemblies? Would it be to just randomly pick 20% of the reads out of the fastq file? Is there a tool out there I could use for this? Thanks, Tom