Runs a canonical correlation analysis using a diagonal implementation of CCA.
For details about stored CCA calculation parameters, see
PrintCCAParams
.
RunCCA(object1, object2, ...)
# S3 method for default
RunCCA(
object1,
object2,
standardize = TRUE,
num.cc = 20,
seed.use = 42,
verbose = FALSE,
...
)
# S3 method for Seurat
RunCCA(
object1,
object2,
assay1 = NULL,
assay2 = NULL,
num.cc = 20,
features = NULL,
renormalize = FALSE,
rescale = FALSE,
compute.gene.loadings = TRUE,
add.cell.id1 = NULL,
add.cell.id2 = NULL,
verbose = TRUE,
...
)
First Seurat object
Second Seurat object.
Extra parameters (passed onto MergeSeurat in case with two objects passed, passed onto ScaleData in case with single object and rescale.groups set to TRUE)
Standardize matrices - scales columns to have unit variance and mean 0
Number of canonical vectors to calculate
Random seed to set. If NULL, does not set a seed
Show progress messages
Assays to pull from in the first and second objects, respectively
Set of genes to use in CCA. Default is the union of both the variable features sets present in both objects.
Renormalize raw data after merging the objects. If FALSE, merge the data matrices also.
Rescale the datasets prior to CCA. If FALSE, uses existing data in the scale data slots.
Also compute the gene loadings. NOTE - this will scale every gene in the dataset which may impose a high memory cost.
Add ...
Returns a combined Seurat object with the CCA results stored.
merge.Seurat
if (FALSE) {
data("pbmc_small")
pbmc_small
# As CCA requires two datasets, we will split our test object into two just for this example
pbmc1 <- subset(pbmc_small, cells = colnames(pbmc_small)[1:40])
pbmc2 <- subset(pbmc_small, cells = colnames(x = pbmc_small)[41:80])
pbmc1[["group"]] <- "group1"
pbmc2[["group"]] <- "group2"
pbmc_cca <- RunCCA(object1 = pbmc1, object2 = pbmc2)
# Print results
print(x = pbmc_cca[["cca"]])
}