Hi all, is there an easier (read: dumbed-down) tutorial for someone wanting to use MAST to do scRNA-seq DEG analysis? I feel comfortable extracting the counts matrix from a Seurat object and converting the 'cell x gene' table into a 'sample x gene' table for pseudobulk approaches (e.g., DESeq2, edgeR, etc.).
However, I'm struggling with the Bioconductor tutorial for MAST as it doesn't start off with a subsetted cluster from a Seurat object (https://www.bioconductor.org/packages/release/bioc/vignettes/MAST/inst/doc/MAITAnalysis.html).
I'm still a beginner, but hoping to benchmark this strategy against the other ones I feel more comfortable with. I've searched through several journals (e.g., Nature) since they generally require authors to submit their code as well, but pretty much all the articles I've come across use MAST within Seurat itself (using FindMarkers) which is not what I want to do. Any advice/tips would be much appreciated!
I try to convert a Seurat object into a SingleCellExperiment object, followed by "SceToSingleCellAssay":
But I get the following error:
I'm not sure what to do there. Any help would be appreciated. Thanks!