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Generate a tri-nucleotide summary for each sliding window
get.toptn(somatic.subset, chr, start.bp, end.bp, ref.dir)
Data frame of somatic variants subset for a specific chromosome
Chromosome
Starting position
Ending position
Path to a directory containing the reference genome.
# NOT RUN { get.toptn(somatic.subset, chr, start.bp, end.bp, ref.dir) # } # NOT RUN { # }
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