bed2dyad | R Documentation |
Single reads will be shifted towards the dyad position assuming an end-localisation of the read For paired reads the fragment mid points will be considered dyad position
bed2dyad(file.id, type = c("SINGLE", "PAIRED"), width = 1)
file.id |
path of the bed file |
type |
sequencing library type "SINGLE" or "PAIRED" |
width |
width of the dyad, default 1 |
the bed files for SINGLE should have columns 1) chromosome 2) start 3) end 4) strand the bed files for PAIRED should have columns 1) chromosome 2) start 3) end
a coverage object (RleList
as returned by coverage
)
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