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Hello,
thanks for maintaining this on github now!
I've been using bbmap stats.sh for quite some time. It works great for contigs as intended (at least on <1million contigs).
Since I like it so much, I tried using it on before and after filtering nanopore read comparisons.
When running on 1-2million reads or more I notice stats getting very wacky and disagreeing with other read and total sequence counting tools
I'll try to find a public read set example. But is there an obvious reason this might be happening (eg using int not long etc in counting functions ?)
Thanks,
Colin
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