Genomics is the study of our genes – the instructions that make us who we are. Changes in these genes can sometimes cause cancer. By looking closely at a patient’s genes, doctors can understand more about their cancer and choose the best treatment.
The NHS offers these tests through Genomic Medicine Services (GMS), making sure everyone has the same access to high-quality testing, no matter where they live.
In Thames Valley, eligible patients can now have genomic tests requested by their local care team. This can mean faster answers and better-informed treatment plans. We work closely with:
- Genomic Laboratory Hubs (GLHs) to ensure equitable access to high-quality testing.
- Genomic Medicine Services to streamline referrals and pathways.
- Primary and secondary care providers to raise awareness of red flags for inherited cancer.
Together, we support clinicians to integrate genomic testing into standard care pathways — from eligibility and consent, to interpretation and management. Our genomics partners can be found here.
The National Genomic Test Directory lists:
- Which tests are available on the NHS.
- How they are done.
- Who can have them.
Genomics Education event: review and materials
Our Genomics Education event on 13 October 2025 organised by TVCA and Macmillan, brought together colleagues and subject experts for a day of insight, discussion, and forward thinking. The sessions covered a wide range of topics, showcasing the depth and diversity of work happening across our teams. Click here to find presentations and photos from the event