This function takes a given GRanges and returns another GRanges object. The new GRanges has the same number of ranges and the same chromosome, width and strand distributions than the original GRanges.
sampleGRanges(
x,
n = NULL,
width = NULL,
exclude = FALSE,
avoid_overlap = FALSE
)
GRanges object
Integer, number of sampled GRanges
Integer, width of sampled GRanges
Boolean, should the original GRanges be excluded?
Boolean, should the sampled GRanges not be overlapping?
A GRanges object of length n
data(ce11_proms)
sampleGRanges(ce11_proms, 100)
#> GRanges object with 100 ranges and 0 metadata columns:
#> seqnames ranges strand
#> <Rle> <IRanges> <Rle>
#> [1] chrI 1610448-1610598 +
#> [2] chrI 2544450-2544600 +
#> [3] chrI 2794866-2795016 +
#> [4] chrI 3864466-3864616 +
#> [5] chrI 6057549-6057699 +
#> ... ... ... ...
#> [96] chrX 14099795-14099945 -
#> [97] chrX 14254630-14254780 -
#> [98] chrX 16527369-16527519 -
#> [99] chrX 17597686-17597836 -
#> [100] chrX 17699646-17699796 -
#> -------
#> seqinfo: 6 sequences from an unspecified genome; no seqlengths