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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