Description Usage Arguments Value
View source: R/genotype_cnps.R
Calculate the likelihood of the observed B allele frequencies for a given copy number model
1 | bafLikelihood(cn.model, snpdata)
|
cn.model |
a copy number model |
snpdata |
a |
a list. The first element is the log likeihood and the second element is the copy number model that maximized the likelihood.
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