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I have two strains of a 3.4 Gb mammalian genome, for which I have good coverage of PacBio and UL ONT generated in house using identical methods. The first strain assembles well to a genome of the expected size, a size consistent with other assemblers' results and with flow cytometry. The second strain assembles into something almost 6 Gb in size, inconsistent with other assemblers and flow cytometry.
I have attached the stderr file for the "bad" genome assembly. Please let me know what additional information I might provide to help figure out why one assembly is bad and the other good.
Thanks,
CB
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