Learn how genome sequencing works
This course will take you behind the scenes to explore this emerging technology and its promises to revolutionise healthcare around the world. 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’.
Explore how whole genome sequencing affects healthcare
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. You will be introduced to England’s pioneering 100,000 Genomes Project and its potential impact on how we understand and care for patients with rare diseases and cancer. You will also discover how genomics is being used in epidemiology and helping us tackle infectious diseases.
You don’t need an in-depth knowledge of genetics, as this course will provide a recap on the basics. It is designed for anyone who wants to learn about whole genome sequencing, how it operates and the impact it is likely to have on healthcare.
The course is aimed at healthcare professionals who have limited or no understanding of the sequencing process and the many varied uses of whole genome sequencing. Science undergraduates and non-specialists who want to learn more about sequencing and genomic medicine are also very welcome.