Screening assembled genomes for contamination using NCBI FCS workflow not working

Hi @Dibya

You won’t need to do that, you can use the workflow, you’ll just need to update it. See the topic I linked. I included a screenshot that shows exactly where to find the tool form Versions menu in the workflow editor. It is the same as a tool form, but the editor is new to some people, so I though it might be helpful.

Here, I’ll copy it

this

Points to

You should give this a try too. Learning how to make small modifications to workflows is really important. Tools change over time, servers may host slightly different versions (as in this case), you may want to use a different reference genome at some point in some workflow, or you may want to extract and create your own. These are really powerful and once you explore it you’ll see it is pretty much like a history but flattened out all at once. Really nice for planning your steps, too.

Let us know how this works! :rocket: