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What? Have you ever looked at a sanger trace with homopolymer stretches? Depending on how blotchy it is, After about 7 you might not really be sure, and it definitely gets the n wrong occasionally even with nicely resolved peaks.

I'm not defending nanopores here, frankly I'm not convinced about them yet.



Sorry, I didn't mean Sanger sequencing, was comparing to Illumina sequencing.




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