Hello,
I was trying to use USEQ's "IntersectRegions" tool to find genomic overlaps. However, I don't think I have understood the concept of "Fold Enrichment" very well. What exactly is "fold enrichment" ? I am aware that it's some kind of "signal over noise" but I'll appreciate it if I can get an explanation of it in simple language.
Also, to calculate fold enrichment, USEQ requires me to use a parameter -r .
They describe it here as follows:
-r Make random regions matched to the second regions file(s) and intersect with the first.
I did not quite understand what "make random regions matched to the second regions file" means.
It'll be great if I could understand this.
Thank you very much. That was very nicely explained :)