```{css, echo=FALSE} .scroll-100 { max-height: 400px; overflow-y: auto; background-color: inherit; }
# Clustering ## Highly variable features ```r obj_scRNA@misc$hvgPlot
List of selected variable genes.
x <- VariableFeatures(object = obj_scRNA) print(x)
Are principal component loaded with cell cycle genes?
obj_scRNA@misc$CC_pca_bar
obj_scRNA@misc$before_cc_pca
obj_scRNA@misc$after_cc_pca
obj_scRNA@misc$elbowPlot
r obj_scRNA@misc$maxPca
principal component and resolution r obj_scRNA@misc$resolution
selected.obj_scRNA@misc$umapPlot if(!is.null(obj_scRNA@misc$markers_info) ){ # DT::datatable(round_df(obj_scRNA@misc$markers_info,digits = 6), rownames = FALSE) DT::datatable(obj_scRNA@misc$markers_info, rownames = FALSE) }else{ print("Cluster markers are not found") }
List of selected variable genes.
obj_scRNA@commands
List of selected variable genes.
sessionInfo()
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