Add a new tutorial explaining how to use breseq to locate a generic integration cassette in a genome.
Use Acinetobacter baylyi ADP1 data and the tdk-Kan cassette as an example.
Show results without providing the cassette reference, with providing it as part of a plasmid, and with annotating it as a repeat_region so it is resolved into a mutation.
There might be some coding to do here to improve things. It would be even better to support prediction of an INT versus a MOB, perhaps depending on how the region was annotated. Maybe features named gene_cassette or integration_cassette or something similar can map to this kind of mutation. Having the distinction could help with mutation counting, screening, etc. Right now, INT mutations must be manually annotated.