Hi IsoQuant team,
I have a single cell Pacbio long read RNA data and would like to use IsoQuant for isoform quantification. I had previously ran the Iso-seq pipeline for pre-processing and had obtained deduplicated mapped bam file with poly-A tail trimmed. I am trying to understand what input file should be used for single cell IsoQuant - should it be unmapped deduplicated bam file with poly-A tail retained? And is there any documentation or recommendations for running single cell IsoQuant?
Thanks a lot for your help!
Best,
Audrey