View source: R/countReadsOverGrangesInBAM.R
count the number of reads over genomic ranges in a BAM file
1 2 3 4 5 6 7 8 9 10 11 | countReadsOverGrangesInBAM(
my_ranges,
bam_file,
bam_type = c("SINGLE", "PAIRED"),
single_read.unique = FALSE,
frag.min = 0,
frag.max = 500,
frag.length = 150,
frag.unique = c("allPAIRED", "oneEND", "bothEND"),
subsampling = 0
)
|
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