title | description | category | subcategory | tags | |
---|---|---|---|---|---|
Seurat Markers |
This code is for finding Seurat markers |
research |
scrnaseq |
|
ssh -XY [email protected]
srun --pty -p interactive -t 0-12:00 --x11 --mem 128G /bin/bash
module load gcc/6.2.0 R/3.4.1 hdf5/1.10.1
R
library(Seurat)
library(tidyverse)
set.seed(1454944673L)
data_dir <- "data"
seurat <- readRDS(file.path(data_dir, "seurat_tsne_all_res0.6.rds"))
Make sure the TSNEPlot looks as expected
TSNEPlot(seurat)
Check markers for any particular cluster against all others
cluster14_markers <- FindMarkers(object = seurat, ident.1 = 14, min.pct = 0.25)
Or look for markers of every cluster against all others
seurat_markers <- FindAllMarkers(object = seurat, only.pos = TRUE, min.pct = 0.25, thresh.use = 0.25)
NOTE: The
seurat_markers
object with be a dataframe with the row names as Ensembl IDs; however, since row names need to be unique, if a gene is a marker for more than one cluster, then Seurat will add a number to the end of the Ensembl ID. Therefore, do not use the row names as the gene identifiers. Use thegene
column.
Save the markers for report generation
saveRDS(seurat_markers, "data/seurat_markers_all_res0.6.rds")