| AlleleFreq | R Documentation | 
Collapses allele counts for each strand and normalize by the total number of counts at each nucleotide position.
AlleleFreq(object, ...)
object | 
 A Seurat object, Assay, or matrix  | 
... | 
 Arguments passed to other methods  | 
Returns a Seurat object with a new assay
containing the allele frequencies for the informative variants.
print("see https://satijalab.org/signac/reference/allelefreq")
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