Participants in Cambridge were keen to highlight the ethical concerns around the storage and dissemination of certain types of data. I just found an interesting article about this at PLoS Genetics: http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000665 with five views on public access to genome-wide data. What are your views more generally on how we balance data protection versus accessibility?