008 - Getting ready for genomic medicine

This is a special edition of Genetics Unzipped, in association with the Genomics Education programme - part of Health Education England. We’ll be finding out how genomic medicine is coming into the NHS, and what it means for everyone working in the health service.

Since the publication of the draft sequence of the human genome back in the early noughties, researchers and doctors have been working hard to harness the secrets within our DNA in order to benefit human health. Progress was slow for several years, due to the high cost and slow pace of sequencing technology. Everything changed with the advent of Next Generation Sequencing in around 2009, making it possible to read the entire sequence of anyone’s genome at low cost and high speed.

To realise the potential of this technology in healthcare, the 100,000 Genomes Project was launched in 2012 aiming to sequence - as you might have guessed - 100,000 genomes from people affected by cancer and rare diseases within the NHS.

The next chapter began in October 2018, when NHS England launched a brand new Genomic Medicine Service, using insights and information from the new era of large-scale DNA sequencing, known as genomics, to improve the nation’s health. The service is aiming to sequence 500,000 whole genomes over the next five years, as part of the UK government’s broader aims to reach five million genomic tests by 2024.

More information and show notes online at Geneticsunzipped.com