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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