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