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reassembling chr0 #41
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It does seem that your chr0 is a little too large. May I ask what genome you are assembling? Also, what is your contig N50? |
Am I interpreting this right by observing that you have a contig N50 of 5k? If you have a large number of very small contigs, those are unlikely to get placed by RaGOO. Only alignments over 1k are even considered. What is the size distribution of contigs that are unplaced? Also, with these difficult plant genomes, minimap2 may not always produce good alignments. What is the distribution of quality values in the 12th column of the If you have the time, you can also try aligning the genome with nucmer. With nucmer, one can set very strict parameters that can sometimes help with polyploid genome alignment. I would recommend |
Hi, Thank you, |
Hi there! The alignments used for scaffolding are in First, run Nucmer to get your delta file and covert the delta file to a PAF format with paftools. Then, just rename that file to Version 2, which will hopefully be ready in the next few months, will allow users to use Nucmer directly. |
Hi,
I ran RaGOO, and 2,288,581,979 bp could be mapped to the reference, but 524,739,651 could not be aligned. How would it be possible to use the unmapped contigs and reassemble them?
Thank you in advance,
Michal
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