I have a list of ranges of genomic regions derived from a series of patients.
> head(dotoo)
GRanges with 6 ranges and 3 metadata columns:
seqnames ranges strand | Id CN Histology
<Rle> <IRanges> <Rle> | <factor> <factor> <factor>
[1] 3 [167946693, 168005541] * | 9 3 MD
[2] 3 [189907623, 189954633] * | 9 3 MD
[3] 6 [132274121, 132384438] * | 9 3 MD
[4] 11 [ 67685096, 70138399] * | 9 4 MD
[5] 12 [ 53859037, 53927595] * | 9 3 MD
[6] 15 [ 19830049, 20089383] * | 9 1 MD
When I plot the genomic aberrations using
autoplot(dotoo, aes(fill=as.factor(Id), color=as.factor(Id)))
I see many overlapping regions, see image
How do find out which regions overlaps between at least 3 patients, and have shared CN
?
Basically, if you look at the picture, how do I find the regions that "stack" over, and only the part that is shared? Is there a way at all?