Hi Kristina,
Rpolicastro is right.
There should be no difference in either using single cell RNA seq data or single nuclear RNA seq data with Seurat.
A good place to start is definitely: https://satijalab.org/seurat/articles/pbmc3k_tutorial.html
Many of the steps are modifiable, based on your judgement. If you know that your data doesn't have any mitochondrial gene contamination, than you could definitely just skip that step.
pbmc[["percent.mt"]] <- PercentageFeatureSet(pbmc, pattern = "^MT-")
VlnPlot(pbmc, features = c("nFeature_RNA", "nCount_RNA", "percent.mt"), ncol = 3)
or the following which I use cause because my expression matrix lists the mitochondrial genes as MT... rather than MT-...
pbmc[["percent.mt"]] <- PercentageFeatureSet(pbmc, pattern = "^MT")
VlnPlot(pbmc, features = c("nFeature_RNA", "nCount_RNA", "percent.mt"), ncol = 3)
just shows the mitochondrial genes.
The subset step where you do:
pbmc <- subset(pbmc, subset = nFeature_RNA > 200 & nFeature_RNA < 2500 & percent.mt < 5)
You can certainly just remove the & percent.mt < 5
(MT gene filtering) to just pbmc <- subset(pbmc, subset = nFeature_RNA > 200 & nFeature_RNA < 2500)
. Furthermore, as you may know the filtering numbers are also up to you to decide where you want to draw the line in QC, based on your analysis of the previous plots generated.
Hope this helps!
Feel free to ask any other questions. I think I've got a decent grasp on Seurat. : )
Sincerely,
Pratik
You can proceed as normal with single nuclei data.