score_avgcn | R Documentation |
Compute the average copy number variation across the genome.
score_avgcn(segments, kit.coverage)
segments |
A |
kit.coverage |
A |
Compute the weighted average (by segment length) of the copy number variation. LOH segments and sexual chromosomes are excluded. Copy number variation is rounded to the next level (1.67 -> 1 but 2.33 -> 3).
A decimal value
score_avgcn(segs.chas_example, oncoscan_na33.cov)
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