Hello All,
I have obtained some scRNAseq data from a repository and the data are in count.matrices.rds files, which appear to be created using dropEst with "-V" option, so each file contains "exon", "intron" and "spanning" (exon/intron spanning) lists of counts.
I was wondering if anyone could advise me on how to turn these lists into a Seurat object? I am used to have "counts", so I'm not sure how to obtain such data from these 3 lists - do I merge them and then use as.Seurat function to turn the result into a Seurat object? If so, how should I merge them?
Thank you very much for your help and advice!
Regards, Anna
Unless you are doing RNA velocity or have another compelling reason, you general use just the exon counts for scRNA-seq. If the data is formatted with features as row names, and cell barcodes as column names, then you can use the Seurat function
CreateSeuratObject
to start the analysis.Thank you very much for your answer! Should I also use the spanning list, since it is "exon/intron spanning", or should I use just the "exon" list?
Thank you in advance!
Regards,
Anna