get_oncoscan_coverage_from_bed | R Documentation |
Load the oncoscan coverage BED file into a GenomicRanges object.
get_oncoscan_coverage_from_bed(filename)
filename |
Path to the coverage BED file. |
Expects the following columns from the BED file (no header): 1. Name of the chromosomal arm (e.g. "1p") 2. Start position of the arm 3. End position of the arm
A GRanges
object containing the regions covered on each
chromosome arm.
oncoscan_na33.cov <- get_oncoscan_coverage_from_bed(
system.file('extdata', 'Oncoscan.na33.r2.cov.processed.bed',
package = 'oncoscanR'))
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