Featured news
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ctDNA for Cancer of Unknown Primary is coming! Webinar on 7 July 2026
From 13 July 2026, patients with CUP can be referred for circulating tumour DNA (ctDNA) testing via the NHS Genomic Test Directory.
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East leads on equitable access to genomic testing for cancer patients
By finding a way to collect samples without the need for specialist technologies, we're helping more patient to benefit from genomic testing.
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New study shows that broader DNA testing is needed to diagnose complex eye conditions
A new study by University of Leicester experts shows that complex eye conditions can be diagnosed much earlier through genome-wide testing.
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Webinar: Empowering nurses and midwives - giving you the tools to improve the care of people with Down syndrome
Our national Genomics Lunch & Learn is series is back.
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Upcoming Genomics Community of Practice sessions
Here at East Genomics we support 16 Genomics Communities of Practice across cancers and rare and inherited conditions. In 2025 we ran over 120 sessions attended by over 1,500 healthcare staff across our region. Our series continues in 2026...
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DNA breakthrough ends 30-year mystery for family with life-threatening heart condition
A family from Nottingham have finally received the correct diagnosis for a dangerous inherited heart condition - after more than three decades of uncertainty - thanks to advances in genetic testing.
All news
ctDNA for Cancer of Unknown Primary is coming! Webinar on 7 July 2026
From 13 July 2026, patients with CUP can be referred for circulating tumour DNA (ctDNA) testing via the NHS Genomic Test Directory.
East leads on equitable access to genomic testing for cancer patients
By finding a way to collect samples without the need for specialist technologies, we're helping more patient to benefit from genomic testing.
New study shows that broader DNA testing is needed to diagnose complex eye conditions
A new study by University of Leicester experts shows that complex eye conditions can be diagnosed much earlier through genome-wide testing.
Webinar: Empowering nurses and midwives - giving you the tools to improve the care of people with Down syndrome
Our national Genomics Lunch & Learn is series is back.
Upcoming Genomics Community of Practice sessions
Here at East Genomics we support 16 Genomics Communities of Practice across cancers and rare and inherited conditions. In 2025 we ran over 120 sessions attended by over 1,500 healthcare staff across our region. Our series continues in 2026...
DNA breakthrough ends 30-year mystery for family with life-threatening heart condition
A family from Nottingham have finally received the correct diagnosis for a dangerous inherited heart condition - after more than three decades of uncertainty - thanks to advances in genetic testing.
Lifesaving genetic stroke test launched in minor stroke clinic at Nottingham University Hospitals
Nottingham University Hospitals (NUH) has become one of a handful of hospitals across the UK to implement a rapid genetic test which could dramatically improve outcomes for thousands of stroke patients in the future.
Feedback sought for WGS in Cancer evaluation
In collaboration with the Cancer Alliances for the East Midlands and East of England we are conducting a formal service evaluation (audit) of the Cancer Whole Genome Sequencing (WGS) pathway.
International Day of the Midwife
Every year on 5 May we celebrate the incredible work of midwives, who play a vital role in supporting families through one of life’s most important journeys.
HNF1B support day, 4 July 2026
The University of Exeter Medical School are hosting an online HNF1B support day in July for patients, families, carers and clinicians.
East of England Cancer Alliance launch first in series of VR training videos
The East of England Regional Genomic Practitioner Service (RGPS) have launched a VR training module called 'Genomics – Mainstream Testing for Lynch Syndrome'.
Reflections on a career in NHS genetics
As she retires, Kim Oakhill, our inherited cancer lead, looks back on a career spanning almost 30 years.
Registration open for ‘Understanding and using the Sickle Cell Clinical Pathway Initiative (CPI)’ webinar
The webinar 'Understanding and using the Sickle Cell Clinical Pathway Initiative (CPI)' will take place on Thursday 21 May 2026 at 11am.
University Hospitals of Leicester national Fragile X Syndrome holistic hub
Co-led by Professor Julian Barwell alongside Chris and Alex McQuade, the University Hospitals of Leicester, in partnership with the Fragile X Society, are establishing a national holistic and integrated care hub.
Our April newsletter out now
Our latest newsletter is now available to read on our website.
Study explores role of somatic mutations in autoimmunity
Trust clinicians and colleagues have shown that accumulated genetic changes could contribute to autoimmunity.
UK study highlights “fragile trust” in healthcare among Black communities
A major UK report has found that trust in healthcare and clinical research among Black communities is strong at a personal level but remains fragile overall, shaped by inequality, past experiences and inconsistent care.
Guidance on blood cancer genetic testing updated following national consensus meeting
Updated guidance follows a 2025 consensus meeting between clinicians, clinical genetics and genomic labs.
Our Generation Study Results Coordinator leads on new infographic for Health Visitors
The Institute of Health Visiting (IHV) are working with Genomics England to support health visitors’ awareness of the Generation Study – a research study run in partnership with NHS England that is testing newborn babies for more than 200 genetic conditions.
Genomic study helps detect baby’s rare growth condition
Baby Safi started treatment for a rare growth condition after participating in the Generation Study, a national genomic screening study