DEGS_scANANSE {AnanseSeurat} | R Documentation |
DEGS_scANANSE
Description
Calculate the differential genes needed for ananse influence
Usage
DEGS_scANANSE(
seurat_object,
output_dir,
min_cells = 50,
cluster_id = "seurat_clusters",
genome = "./scANANSE/data/hg38",
RNA_count_assay = "RNA",
additional_contrasts = "None"
)
Arguments
seurat_object |
seurat object |
output_dir |
directory where the files are outputted |
min_cells |
minimum of cells a cluster needs to be exported |
cluster_id |
ID used for finding clusters of cells |
genome |
path to the genome folder used for the anansnake config file |
RNA_count_assay |
assay containing the RNA data |
additional_contrasts |
additional contrasts to add between clusters within cluster_ID |
Value
None, outputs DEG files in the output directory
Examples
sce_small <- readRDS(system.file("extdata","sce_obj_tiny.Rds",package = 'AnanseSeurat'))
DEGS_scANANSE(sce_small, min_cells = 2, output_dir = tempdir())
[Package AnanseSeurat version 1.2.0 Index]