Let's say we have the following situation.
We have a unique breakpoint in mtDNA (a deletion in the mtDNA). If by chance this molecule is replicated and now this unique molecule exist as multiple copies.
How would delly handle this situation? Can it distungish how many molecules exits in the sample? if by counting this unique breakpoint only once with the software, is it be possible that we are not considering the abundance of this unique breakpoint.
I would appreciate any hints also as to where I can look it up.
thanks
Assa
thanks for the explanation, but this was not my question. I am not interested in the biology behind it. I would like to know if, when using the tool delly for quantifying breakpoints, the problematic of having the same molecules multiple times is accounted for.
Can delly quantify the number of copies, or just output how many breakpoints exit in the data set?
thanks
I'm a bit confused. Usually variant callers like Delly would give a "depth" parameter for the variants. Isn't that what you're looking for? Of course, "depth" is not number of copies or number of molecules, they're just related. You need other approaches to track down the number of molecules.