scROSHI identifies cell types based on expression profiles of single cell analysis by utilizing previously obtained cell type specific gene sets. It takes into account the hierarchical nature of cell type relationship and does not require training or annotated data. A detailed description of the method can be found at: Prummer et al. 2022. “scROSHI - robust supervised hierarchical identification of single cells”. bioRxiv. https://www.biorxiv.org/content/10.1101/2022.04.05.487176v1
You can install the development version from GitHub (required R version >= 3.6) with:
# install.packages("devtools")
::install_github("ETH-NEXUS/scROSHI") devtools
This is a basic example for the scROSHI function
scROSHI requires three input objects:
sce_data
A SingleCellExperiment object containing the expression profiles of the single cell analysis
celltype_lists
Marker gene list for all cell types. It can be provided as a list of genes with cell types as names or as a path to a file containing the marker genes. Supported file formats are .gmt or .gmx files.
type_config
Config file to define major cell types and hierarchical subtypes. It should be provided as a two-column data.frame where the first column are the major cell types and the second column are the subtypes. If several subtypes exists they should be separated by comma.
library(scROSHI)
data("test_sce_data")
data("config")
data("marker_list")
<- scROSHI(sce_data = test_sce_data,
results celltype_lists = marker_list,
type_config = config)
table(results$celltype_final)
#>
#> B.cells B.cells.naive
#> 4 180
#> B.cells.precursor Dendritic.cells
#> 40 40
#> Monocytes NK.cells
#> 233 219
#> Plasma.cells Plasmacytoid.dendritic.cells
#> 13 11
#> T.cells T.cells.CD4
#> 60 415
#> T.cells.CD8 uncertain
#> 76 25