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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) }
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