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Miniasm is designed for reads. It filters out reads with low coverage. You can see all input sequences are dropped at step 4. You may try to add option -1 -2 (or just -2). I don't know if that helps, though.
I like to combine different metagenome-assembled genomes (contigs) into one.
I tried to use miniasmwith:
The gfa file is empty and I get the following log.
The text was updated successfully, but these errors were encountered: