Sage Bionetworks hopes 25,000 people will sign up in the first year, either because trialorganisers choose to adopt the protocol or volunteers insist on it. But to be really useful, the database would need to grow to ten or 100 times this size. Mr Wilbanks has therefore started discussions with several firms that offer commercial genetic tests for a range of diseases. It is also linking up with PatientsLikeMe, an organisation that helps almost 150,000 people find those with similar illnesses, in order to share their experiences.
Are we all agreed?
So far, the Portable Legal Consent is valid only in America, although Sage Bionetworks is looking at ways of adapting it to fit the legal frameworks of China and the European Union. How quickly the idea will catch on remains to be seen. But if it does, other sorts of researchers who rely on gathering personal data—for example in sociology or in tracking energy use in homes—may find itattractive. And that would enable research of a sort that is now impossible, by opening up the field of quantifiable social science.