View source: R/supercell_FindAllMarkers.R
supercell_FindMarkers | R Documentation |
Differential expression analysis of supep-cell data. Most of the parameters are the same as in Seurat FindMarkers (for simplicity)
supercell_FindMarkers(
ge,
supercell_size = NULL,
clusters,
ident.1,
ident.2 = NULL,
genes.use = NULL,
logfc.threshold = 0.25,
min.expr = 0,
min.pct = 0.1,
seed = 12345,
only.pos = FALSE,
return.extra.info = FALSE,
do.bootstrapping = FALSE
)
ge |
gene expression matrix for super-cells (rows - genes, cols - super-cells) |
supercell_size |
a vector with supercell size (ordered the same way as in |
clusters |
a vector with clustering information (ordered the same way as in |
ident.1 |
name(s) of cluster for which markers are computed |
ident.2 |
name(s) of clusters for comparison. If |
genes.use |
set of genes to test. Defeult – all genes in |
logfc.threshold |
log fold change threshold for genes to be considered in the further analysis |
min.expr |
minimal expression (default 0) |
min.pct |
remove genes with lower percentage of detection from the set of genes which will be tested |
seed |
random seed to use |
only.pos |
whether to compute only positive (upregulated) markers |
return.extra.info |
whether to return extra information about test and its statistics. Default is FALSE. |
do.bootstrapping |
whether to perform bootstrapping when computing standard error and p-value in wtd.t.test |
a matrix with a test name (t-test), statisctics, adjusted p-values, logFC, percenrage of detection in eacg ident and mean expresiion
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