knitr::opts_chunk$set( collapse = TRUE, comment = "#>" ) # reduce the minimum number of characters for the tibble column titles (default: 15) options(pillar.min_title_chars = 10)
The clustermole R package is designed to simplify the assignment of cell type labels to unknown cell populations, such as scRNA-seq clusters. It provides methods to query cell identity markers sourced from a variety of databases. The package includes three primary features:
clustermole_markers()
)clustermole_overlaps()
)clustermole_enrichment()
)You can install clustermole from CRAN.
install.packages("clustermole")
Load clustermole.
library(clustermole)
You can use clustermole as a simple database and get a data frame of all cell type markers.
markers <- clustermole_markers(species = "hs") markers
Each row contains a gene and a cell type associated with it.
The gene
column is the gene symbol and the celltype_full
column contains the full cell type string, including the species and the original database. Human or mouse versions can be retrieved.
Many tools that works with gene sets require input as a list.
To convert the markers from a data frame to a list, you can use gene
as the values and celltype_full
as the grouping variable.
markers_list <- split(x = markers$gene, f = markers$celltype_full)
If you have a character vector of genes, such as cluster markers, you can compare them to known cell type markers to see if they overlap any of the known cell type markers (overrepresentation analysis).
my_overlaps <- clustermole_overlaps(genes = my_genes_vec, species = "hs")
If you have expression values, such as average expression for each cluster, you can perform cell type enrichment based on the full gene expression matrix (log-transformed CPM/TPM/FPKM values).
The matrix should have genes as rows and clusters/samples as columns.
The underlying enrichment method can be changed using the method
parameter.
my_enrichment <- clustermole_enrichment(expr_mat = my_expr_mat, species = "hs")
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