Closed malonzm1 closed 1 year ago
The aligned reads are retained in the .bam
or .pro
alignment file, but those contain only biological and not technical sequences. Most likely you would have to go back to the original sequencing dataset and re-process it to single cells and analyze them again.
Serratus is not set-up or intended to work with scRNAseq data, you can try Vulture, although I've never used it.
Hi,
I'm performing Serratus/Tantalus analysis with scRNA-seq data. Each sample/fastq file consists of several cells. What I'd like to do is to map the output viral info to an individual cell. Is this possible?
Thanks and good day.