The key ethical issues really relate to expectations, managing expectations properly and an understanding of what can be delivered and what can't be delivered. With the 100,000 Genomes Project is the opportunity for three groups of patients – so cancer, rare diseases, and infectious diseases – to access sequencing technology. By doing that, they may gain answers to a diagnosis, to a range of treatments that are possible for them, or they may gain absolutely nothing. The promise of the delivery of answers is really bandied around but actually, may not offer nothing useful at all. I think patients seems to go in and engage with it with their eyes open. As in any genetic test, if you get results related to anything, the results are often relevant to not only yourself but also to your immediately family as well – so your siblings, your parents, your children. So, patients may go for a test for one thing and come out with answers relevant to their whole family. And so, that raises ethical dilemmas for different people and so it sort of really brings to the heart of this that consent is the most important thing, and that people really understand what it is that they're signing up for, they understand what the options are in terms of results, and they go into it with their eyes open.