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                                            hkarakurt8742

Generating Single VCF file for Each scRNA-Seq Sample

> Hi, thanks for the question. > > Yes, you can call the variants in a pseudobulk manner on the cellranger BAM file. However, it is recommended to subset the...

Using CaSpER with single bulk RNA-Seq sample

> @hkarakurt8742 Hi, did you manage to do it with a single sample? I could not actually. I could not find any method to do it.