Hi !

I'm new using CheckM and I wondered if you had any tips to have a quick overvue of ckeckM analysis. I run the lineage specific workflow on a single genome with that command : checkm lineage_wf folder_with_fnafile checkm_output and I got as a results a lot of files with different results. Do you know a simple way to observe them (for me the priority would be to see the genome completeness) ?

Thank you for your help, Sofia