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
I was interested in how the LCBs called by SibeliaZ change as I include more genomes, so to start, I ran it with two ~4.5Mb genomes that differed only by a single ~10kb inversion that I introduced. I expected to see something like 3 LCBs since the sequences are otherwise identical, but I was getting around 2100. I can't find anything in the algorithm description in your paper to explain this. There should only be bubbles in the vicinity of the inversion that I introduced, but nowhere else. Is the large number of LCBs for these near-identical genomes expected behavior, and how?
The text was updated successfully, but these errors were encountered:
I was interested in how the LCBs called by SibeliaZ change as I include more genomes, so to start, I ran it with two ~4.5Mb genomes that differed only by a single ~10kb inversion that I introduced. I expected to see something like 3 LCBs since the sequences are otherwise identical, but I was getting around 2100. I can't find anything in the algorithm description in your paper to explain this. There should only be bubbles in the vicinity of the inversion that I introduced, but nowhere else. Is the large number of LCBs for these near-identical genomes expected behavior, and how?
The text was updated successfully, but these errors were encountered: