Hi,
I have a dataset containing both short- and long-read RNAseq data(ONT). Can I correct errors in the long-read RNAseq data by integrating short-read RNAseq data? Have you tried any software for that, and could you recommend any?~
Hi, can't comment on that - this workflow has been set up and tested for use with long-read Nanopore data, perhaps pose this question in the community.
Ask away!
Hi, I have a dataset containing both short- and long-read RNAseq data(ONT). Can I correct errors in the long-read RNAseq data by integrating short-read RNAseq data? Have you tried any software for that, and could you recommend any?~