Contact FutureLearn for Support Whole Genome Sequencing - Free online course Skip main navigation
We use cookies to give you a better experience, if that’s ok you can close this message and carry on browsing. For more info read our cookies policy.
We use cookies to give you a better experience. Carry on browsing if you're happy with this, or read our cookies policy for more information.
Watch the trailer
Download video: standard or HD
About the course

Whole genome sequencing is a relatively new technology that allows us to ‘read’ a person’s or organism’s entire genetic code. But how does it work and what does it mean for all of us? How do scientists begin to make sense of the vast amount of information that whole genome sequencing provides? And what does this new technology mean for the future of healthcare and personalised medicine?

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.

Requirements

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.

Buy a personalised, digital and printed certificate and transcript

You can buy a Certificate of Achievement for this course — a personalised certificate and transcript in both digital and printed formats, to prove what you’ve learnt. A Statement of Participation is also available for this course.

Certificate of Achievement + transcript £69.00

Statement of Participation £39.00

Estimate prices in preferred currency

Charges to your account will be made in GBP. Prices in local currency are provided as a convenience and are only an estimate based on current exchange rates.

Course highlights Get a taste of this course before you join: