Craig Campbell, an esteemed colleague, has a Canadian neuromuscular disease registry that is run out of Calgary. It is a very impressive disease registry, where you can track safety and do clinical trials. It's a perfect model for how things should be done in a perfect world.
I think as we go ahead with the companies and new drugs being introduced, an important part is setting up these networks and capturing the data as we go forward, ensuring efficacy and ensuring safety. I know the that the CNDR is in conversation with Biogen on spinal muscular atrophy, for example.
I think that's an absolutely important aspect that we need to do, ultimately not to sort of perseverate with the Genome Canada project, but the introduction of these rare disease genomes is going to be a good platform from which to move on to registries as well.