Dear mailing list,
I have a metagenome of about 2.5B reads of 150 length. If I choose to use the
meta ray assembler, what would be the parameters that could
influence the running time and computational resources (assuming the
genomes comprising the metagenomes follow power law)?Is there a log in which I
can monitor the progress of my job?
Tank you very much,
Sheerli
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