Consent
After reading information about the BioResource and given the opportunity to ask any questions, volunteers provide consent for their samples and personal information to be collected. Participants will also grant the BioResource team access to their medical records, but these will only be accessed if required for a particular study.
DNA Samples
Volunteers are asked to provide a DNA sample to the BioResource. This is usually collected via a blood sample, but in some cases saliva may be used instead. These samples are then sent for testing and storage, and genetic information is added to a national database. Samples are kept separately from personal information such as name, address and date of birth and all information is protected by national governance and ethics policies.
Health and Lifestyle Questionnaire
Volunteers complete a simple health and lifestyle questionnaire. This helps match volunteers to potential research studies.
Researcher Requests
Researchers can then request access to the stored genetic information or the original samples for their work. Volunteers may be selected based on variations in their DNA, their health and lifestyle information, their age, their ethnicity or their gender.
Volunteer Invites
If matched, volunteers are contacted to ask if they wish to take part in the study. Each volunteer can be invited to up to 8 studies per year, with a maximum of 4 being face-to-face. There is no obligation to take part in any study that they are invited to, and not taking part in a study will have no effect on their potential to be invited to future studies.