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I have a bactieria genome sequencing data set which contains an previous NGS assemblied contigs(raw data missed) and recently nanopore sequencing data, so I want fill gaps of ngs contigs with nanopore data assembly genome(using flye and get a complete contig), I first use ragtag scaffold module combines NGS contigs with nanopore assembly genome and get a gap filling contig(and with several sites of Ns nearly 50 Kb in sum),
Hi,
I have a bactieria genome sequencing data set which contains an previous NGS assemblied contigs(raw data missed) and recently nanopore sequencing data, so I want fill gaps of ngs contigs with nanopore data assembly genome(using flye and get a complete contig), I first use ragtag
scaffold
module combines NGS contigs with nanopore assembly genome and get a gap filling contig(and with several sites of Ns nearly 50 Kb in sum),Then try to fill these Ns with
patch
module with or without set--fill-only
.But both can not eliminate Ns, is there anything wrong with above commands?
Thanks
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