Closed btemperton closed 6 years ago
Speaking from my own experience, it should not matter how long the contigs are. Just bear in mind that the very flanking tips of contigs (e.g. first and last 20-30bp) may not get corrected.
@nickloman is right, polishing small contigs should work fine except for the very ends
We have a viral metagenome sequenced by 1D ligation and assembled in canu. Canu + PILON gets us within 99% ANI of contigs we see from SPAdes hybrid assemblies. I would like to try CANU + nanopolish + PILON to see if (a) we can get closer (see http://albertsenlab.org/what-is-a-good-genome-assembly/) and (b) if we can detect any methylation signal in the viral genomes. However, even if we manage to sequence complete viral genomes, most of the contigs will be 10-300kb. What effect will this have on nanopolish?