dataDir <- system.file("extdata",package="flowWorkspaceData")
gs <- load_gs(list.files(dataDir, pattern = "gs_manual",full = TRUE))
# default is "both"
p <- ggcyto(gs, aes(x = CD4, y = CD8), subset = "CD3+") + geom_hex(bins = 64)
p
#use marker name as x,y labs
p + labs_cyto("marker")
#use channel name as x,y labs
p + labs_cyto("channel")
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