# \dontshow{
options(gmax.processes = 2)
# }
gdb.init_examples()
# Create some intervals
intervs1 <- gscreen("dense_track > 0.15")
intervs2 <- gintervals(c("chr1", "chr2"), 0, c(100000, 100000))
# Calculate fraction of intervs2 covered by intervs1
gintervals.coverage_fraction(intervs1, intervs2)
# Calculate fraction of entire genome covered by intervs1
gintervals.coverage_fraction(intervs1)
Run the code above in your browser using DataLab