I did RNA-seq analysis and I have the plant genome and GFF files. However, I need to add to these files the bacterial sequences that I used to have my transgenes. The genome file is too big (3.6gb) so I don’t know how to open it. Do you have any suggestions?
In short, combine the fasta for the two different organisms, then add in some lines to the existing reference annotation to represent the extra genes/transgenes. This will take some trial and error to get right.
Working with a 4 GB file is fine when doing data manipulations in Galaxy.