Direct RNA-seq Nanopore
I want to perform directed RNA-seq Nanopore-derived data and I was not sure if I should use dorado simplex basecaller and then minimap2 to align reads to reference transcriptome or use besacaller aligner function directly. Should I have to take more aspects into account in order to establish a specific data analysis pipeline?
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Can you confirm that you are looking to do direct RNA sequencing that is "adaptive" i.e. for only certain genes you are interested in?
Adaptive sequencing can be tricky with nanopore and the last I knew, direct RNA was not being used for this method.
doradousesminimap2under the covers to do the alignments so either way should be fine. You will need to make sure the presetsdoradouses match the ones you do.