Whole genome sequencing is a relatively new technology that allows us to ‘read’ a person’s or organism’s entire genetic code. You will be given a unique insight into modern genetics laboratories and state of the art sequencing facilities, led by clinical scientists who are using whole genome sequencing to shape decisions about patient care and appropriate treatments. You will be introduced to the fundamental basics of DNA and genetic variation, before exploring the process of whole genome sequencing and the ways in which the resultant data can be analysed and used to benefit patients. Leading scientists and genomics experts will explore the potential and limitations of this new technology, and the ethical questions that arise when we can ‘read a person’s genome’. Throughout the course you will be introduced to a range of case studies and scenarios where whole genome sequencing is having a profound impact on healthcare and life decisions.