bam2coverage | R Documentation |
Reads can optionally be filtered by a chromosome inclusion list Single reads will be extended to the provided fragment length
bam2coverage(file.id, type = c("SINGLE", "PAIRED"), fragment.length = 200,
chr.flt = NA)
file.id |
path of the bam file |
type |
sequencing library type "SINGLE" or "PAIRED" |
fragment.length |
average chromatin fragment size, default 200 |
chr.flt |
vector of chromosome names to be included |
a coverage object (RleList
as returned by coverage
)
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