Megalodon is a research command line tool to extract high accuracy modified base and sequence variant calls from raw nanopore reads by anchoring the information rich basecalling neural network output to a reference genome/transriptome.
Hi, I have run Megalodon on different subfolders and I merged all the outputs (per_read_modified_base), as I have different reads, I want to aggregate them using megalodon_extras aggregate. Can I do it without running it again? If true, what parameters are needed?
Hi, I have run Megalodon on different subfolders and I merged all the outputs (per_read_modified_base), as I have different reads, I want to aggregate them using megalodon_extras aggregate. Can I do it without running it again? If true, what parameters are needed?
Thank you :)