Hi, I am working with a genome de novo assembled based on PacBio reads. I have a FASTA formatted polished genome sequence, and a GFF3 file containing information on the modified bases (methylation patterns). Is there a way to load these in Artemis? It seems Artemis only handles "feature keys" in the type "column", meaning I can only input "modified_base". It seems the only way to incorporate the type of modification would be to use the "Attributes" column for that? Any input is welcome.
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