Why did you choose to start with plasmid origins and selectable markers?
It’s not obvious to me that that’s the limiting step. You listed a bunch of other things you did during the postdoc, ie closed genome, delivery (and molecular) tools, functional annotations
Why did you choose to start with plasmid origins and selectable markers?
It’s not obvious to me that that’s the limiting step. You listed a bunch of other things you did during the postdoc, ie closed genome, delivery (and molecular) tools, functional annotations
Why not start with any of those?