Load gene expression count data
read10x(
data.path,
samples = NULL,
raw = FALSE,
symbol = TRUE,
sep = "!!",
unique.names = TRUE,
n.cores = 1,
verbose = TRUE
)
data frame
Path to cellranger count data.
Vector of sample names (default = NULL)
logical Add raw count matrices (default = FALSE)
The type of gene IDs to use, SYMBOL (TRUE) or ENSEMBLE (default = TRUE).
Separator for cell names (default = "!!").
Number of cores for the calculations (default = 1).
Print messages (default = TRUE).
if (FALSE) {
cms <- read10x(data.path = "/path/to/count/data",
samples = crm$metadata$samples,
raw = FALSE,
symbol = TRUE,
n.cores = crm$n.cores)
}
Run the code above in your browser using DataLab