findMarkerGenes: Identify marker genes for each cluster.

View source: R/SingleCellRNASeq.R

findMarkerGenesR Documentation

Identify marker genes for each cluster.

Description

Identify marker genes for each cluster.

Usage

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
)

Arguments

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.


supatt-lab/SingCellaR documentation built on Aug. 24, 2023, 5:49 p.m.