Im trying to get at the rough structure of a genomic region. My coverage of this region is extremely low (3x). I simply want to see how my reads stack up with one another, I don't need high-confidence assembly.
What would be a good way to stitch together these very low coverage reads? Even if there is a 2-read contig, that is sufficient. My reads are quite long (N50 35kb), using nanopore.
I have been using:
-x ont -t 16 -S 1 -l 1000 --edge-min 1 --rescue-low-cov-edges -R --no-read-clip --aln-dovetail
Hi,
Im trying to get at the rough structure of a genomic region. My coverage of this region is extremely low (3x). I simply want to see how my reads stack up with one another, I don't need high-confidence assembly. What would be a good way to stitch together these very low coverage reads? Even if there is a 2-read contig, that is sufficient. My reads are quite long (N50 35kb), using nanopore.
I have been using: -x ont -t 16 -S 1 -l 1000 --edge-min 1 --rescue-low-cov-edges -R --no-read-clip --aln-dovetail
Thanks!