You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Hi,
I tried to assemble circular DNA with hifi reads, and made it.
I found overlapping region of contig with width about 22 kbp using nucmer. (total contig length = 878,387bp)
My question is that, why this overlapping region is made in specific region?
How canu define the seed reads to start assembly and end..?
I have been studying canu but cannot find it well.
Thank you for your time, and I look forward to your response.
The text was updated successfully, but these errors were encountered:
Circular molecules typically generate self-similar sequences at the start and end, see https://canu.readthedocs.io/en/latest/faq.html#my-circular-element-is-duplicated-has-overlap. This is because the start of the molecule is arbitrarily defined (there's no start/end on a circle) and reads are not split so the end read can repeat the start sequence again. Typically, canu will mark these as circular in the header and provide trim coordinates to remove the redundancy.
Hi,
I tried to assemble circular DNA with hifi reads, and made it.
I found overlapping region of contig with width about 22 kbp using nucmer. (total contig length = 878,387bp)
My question is that, why this overlapping region is made in specific region?
How canu define the seed reads to start assembly and end..?
I have been studying canu but cannot find it well.
Thank you for your time, and I look forward to your response.
The text was updated successfully, but these errors were encountered: