View source: R/cellmarker_enrich.R
cellmarker_enrich | R Documentation |
This function uses the CellMarker and Panglao datasets to identify cell-type differentially expressed genes.
cellmarker_enrich(
gene_list,
p_thresh,
gmt = "cellmarker_list.Rdata",
fixed_length = 13000,
min_genes = 5,
max_genes = 3000,
isect_size = 3
)
gene_list |
A character vector of gene symbols with the same designation (e.g. mouse symbol - mouse, human symbol - human) as the gene set database. |
p_thresh |
The Fisher's test cutoff for a cell-marker to be enriched. |
gmt |
Either a path to an rda file containing an object called "gmt", which is a named list where each element of the list is a vector of gene symbols website for more detail on the file type (https://software.broadinstitute.org/cancer/software/gsea/wiki/index.php/Data_formats). The gmt list may also be inputted. |
fixed_length |
Estimated number of genes in your background. |
min_genes |
Minimum number of genes in the cell-type markers. |
max_genes |
Maximum number of genes in the cell-type markers. |
isect_size |
Number of genes in your list and the cell-type. |
Complete a Fisher's exact test of an input list of genes against a gene set saved in an *.RData object. The RData object is storing a named list of genes called "gmt".
cellmarker_enrich
Gene set enrichment of cell-types on your inputted gene list.
data(POA_example)
POA_generes <- POA_example$POA_generes
POA_OR_signature <- POA_example$POA_OR_signature
POA_Rank_signature <- POA_example$POA_Rank_signature
Signature <- POA_Rank_signature
rowname <- get_gene_symbol(Signature)
rownames(Signature) <- rowname$rowname
genes <- rownames(Signature)[1:100]
data(gmt)
enriched <- cellmarker_enrich(gene_list = genes,
p_thresh = 0.05, gmt = gmt)
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.