Dear developers, thank you for the program. It looks promising judging by the article. But I am interested in a detailed manual of various settings. I have a routine task to assemble viral contigs from lake metagenome from fraction less than 0.2 µm. How do I figure out which settings will help me for best results? My project PRJNA1006167
Dear developers, thank you for the program. It looks promising judging by the article. But I am interested in a detailed manual of various settings. I have a routine task to assemble viral contigs from lake metagenome from fraction less than 0.2 µm. How do I figure out which settings will help me for best results? My project PRJNA1006167