View source: R/SingleCellRNASeq.R
| findMarkerGenes | R Documentation | 
Identify marker genes for each cluster.
findMarkerGenes(
  object,
  cluster.type = c("louvain", "walktrap", "kmeans", "merged_walktrap", "merged_louvain",
    "merged_kmeans"),
  min.log2FC = 0.5,
  min.expFraction = 0.3,
  limit.top.genes = 500,
  use.sampling.cells = FALSE,
  use.fraction.of.cells = 0.2,
  n.seed = 1
)
| object | The SingCellaR object. | 
| cluster.type | The type of clustering method. | 
| min.log2FC | The minimum cutoff of the log2FC. Default 0.5 | 
| min.expFraction | The minimum expressing cells fraction. Default 0.3 | 
| limit.top.genes | The limited number of differential genes to be shown. Default 500 | 
| use.sampling.cells | is logical. If TRUE, the downsample cells will be processed. | 
| use.fraction.of.cells | The fraction of downsample. Default 0.2 | 
| n.seed | The number of set seed. | 
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