Hi All,
I would like to know if it is possible to use bedtools to count the number of occurrences where a feature from set A and set B overlap with a feature in set C (but don't necessarily overlap with each other).
For example, if datasets A and B are bed files from Chip-seq experiments and C defines a set of genomic regions (for example +/- 2kb around TSSs) is there a way to count the number of times that a region in A and B are found overlapping with a region in C but don't necessarily intersect with each other?
To clarify, can you provide an example input and the output you want to get from it?