custom_marker
data.frame and then use it in findmarkergene()
e.g., scRNA-seq data from rat
custom_marker <- data.frame(species = c("Rat", "Rat", "Rat", "Rat"),
tissue = c("Liver", "Liver", "Liver", "Liver"),
cancer= c("Normal", "Normal", "Normal", "Normal"),
condition = c("Normal cell", "Normal cell", "Normal cell", "Normal cell"),
subtype1 = c("NA", "NA", "NA", "NA"),
subtype2 = c("NA", "NA", "NA", "NA"),
subtype3 = c("Periportal", "Periportal", "Pericentral", "Pericentral"),
celltype = c("Hepatocyte", "Hepatocyte", "Hepatocyte", "Hepatocyte"),
gene = c("Cyp2f2", "Alb", "Glul", "Cyp2e1"),
resource = c("Experiment", "Experiment", "Experiment", "Experiment"),
pmid = c("28166538", "28166538", "28166538", "28166538"), stringsAsFactors = FALSE)
obj <- findmarkergene(object = obj, species = "Rat", marker = custom_marker, tissue = "Liver")
RetroSearch is an open source project built by @garambo | Open a GitHub Issue
Search and Browse the WWW like it's 1997 | Search results from DuckDuckGo
HTML:
3.2
| Encoding:
UTF-8
| Version:
0.7.4