find_markers | R Documentation |
Find marker genes for cell clusters using scran findMarkers
find_markers( sce, clusters, annot, block = NULL, lfc = 1, test.type = c("t", "wilcox", "binom"), direction = c("up", "down", "any"), pval.type = c("any", "all"), assay_type = c("logcounts", "counts", "corrected"), ncores = 1, fdr_cutoff = 0.25, prefix = NULL, write = TRUE )
sce |
A SingleCellExperiment object containing expression values, usually counts. |
clusters |
Vector specify cell clusters. |
annot |
gene annotation. |
block |
Vector specify blocking. |
lfc |
Log fold-change. |
test.type |
String specifying the type of pairwise test to perform -
a t-test with |
direction |
Direction of change. |
pval.type |
A string specifying how p-values are to be combined across pairwise comparisons for a given group/cluster. |
assay_type |
A string specifying which assay values to use, e.g., "counts" or "logcounts". |
ncores |
Number of cores. |
fdr_cutoff |
FDR cutoff for top marker genes. |
prefix |
Prefix for file name for the QC metrics histograms. |
write |
TRUE/FASLE for whether write the table of filtered cells. |
A data.frame for the statistics and annotation of top marker geness
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.