Hello,
I've run sliding window Chromunity at 25 kb resolution. Looking at the results, I noticed that there are some binsets with identical ranges, but they were called in adjacent, overlapping windows so their binid/chid differ. When I look at their concatemers, some duplicated binsets have the same reads mapped to them, but others have different reads.
How do you suggest handling these duplicates for synergy and other downstream analyses (e.g. comparing methylation in synergistic vs non-synergistic regions)?
Thank you!
Hello,
I've run sliding window Chromunity at 25 kb resolution. Looking at the results, I noticed that there are some binsets with identical ranges, but they were called in adjacent, overlapping windows so their binid/chid differ. When I look at their concatemers, some duplicated binsets have the same reads mapped to them, but others have different reads.
How do you suggest handling these duplicates for synergy and other downstream analyses (e.g. comparing methylation in synergistic vs non-synergistic regions)?
Thank you!