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Identify mitochondrial variants present in single cells.
IdentifyVariants(object, ...)# S3 method for default IdentifyVariants( object, refallele, stabilize_variance = TRUE, low_coverage_threshold = 10, verbose = TRUE, ... )# S3 method for Assay IdentifyVariants(object, refallele, ...)# S3 method for StdAssay IdentifyVariants(object, refallele, ...)# S3 method for Seurat IdentifyVariants(object, refallele, assay = NULL, ...)
# S3 method for default IdentifyVariants( object, refallele, stabilize_variance = TRUE, low_coverage_threshold = 10, verbose = TRUE, ... )
# S3 method for Assay IdentifyVariants(object, refallele, ...)
# S3 method for StdAssay IdentifyVariants(object, refallele, ...)
# S3 method for Seurat IdentifyVariants(object, refallele, assay = NULL, ...)
Returns a dataframe
A Seurat object
Arguments passed to other methods
A dataframe containing reference alleles for the mitochondrial genome.
Stabilize variance
Low coverage threshold
Display messages
Name of assay to use. If NULL, use the default assay.
if (FALSE) { data.dir <- "path/to/data/directory" mgatk <- ReadMGATK(dir = data.dir) variant.df <- IdentifyVariants( object = mgatk$counts, refallele = mgatk$refallele ) }
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