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working with genome grist output and realizing that contaminated eukaryotic genomes (where, e.g., deep sequencing of eukaryotic isolates from fecal samples) will likely throw sourmash gather through a loop because the set-cover algorithm will decide to allot a LOT of k-mers there bc there are many/multiple genomes. we are seeing this with some wastewater searches of emerging pathogens (e.g., cyclospora cayatenensis)
not really a sourmash problem, but helpful to consider and report.
The text was updated successfully, but these errors were encountered:
hi there-- hope you're well!
working with genome grist output and realizing that contaminated eukaryotic genomes (where, e.g., deep sequencing of eukaryotic isolates from fecal samples) will likely throw sourmash gather through a loop because the set-cover algorithm will decide to allot a LOT of k-mers there bc there are many/multiple genomes. we are seeing this with some wastewater searches of emerging pathogens (e.g., cyclospora cayatenensis)
not really a sourmash problem, but helpful to consider and report.
The text was updated successfully, but these errors were encountered: