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.
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More than 100 children with cancer across the East of England benefit from whole genome sequencing
In a significant milestone, more than 100 children with cancer from across the East of England have had their tumours tested by whole genome sequencing (WGS) and interpreted by scientists in the NHS Genomic Medicine Service at Cambridge University Hospitals NHS Foundation Trust (CUH), to help improve their diagnosis and treatment.
Largest study of whole genome sequencing data reveals new causes of cancer
Cambridge analysis of more than 12,000 tumours from NHS patients has found DNA evidence of over 50 new potential causes of cancer.
Revolutionary new treatment path for patients with aggressive brain tumours
Brain tumour patients at Addenbrooke’s Hospital in Cambridge are the first in the UK to benefit from personalised treatment using the latest advances in genomics and targeted therapies through the Minderoo Foundation's new Precision Brain Tumour Programme (MPBTP).
Genetic testing for Lynch syndrome help patients and clinicians fight cancer
Awareness of this inherited condition can help patients alert relatives to get tested and it can also ensure suitable screening and preventative treatment for future cancers
With a history of cancer in the family, Marla's story highlights how a Lynch syndrome diagnosis has helped her
Marla explains how she can look forward and concentrate on the prevention of cancer for herself and her family since her Lynch syndrome diagnosis
Genetic study gives new insights into severe Covid
The world’s largest genetic study of critically-ill Covid patients, involving more than 200 treated at Addenbrooke's, reveals extensive insights into the disease.
Family share Eilidh's story on Rare Disease Day
Raising a child with a rare or little understood condition is a major challenge for parents.
E-learning modules launched to help clinicians across the region order genomic tests for patients
Clinical Geneticists and Genetic Counsellors at Cambridge University Hospitals (CUH) have developed several short e-learning modules to help healthcare professionals across the East of England and East Midlands offer genomic testing to patients.
Cambridge clinician wins funding to safely link big datasets to help find medical answers
Cambridge researchers are to trial methods of analysing data across more than one secure research environment – something which has previously not been possible, but which could be of great benefit to the public once established.
Whole genome sequencing improves diagnosis of rare diseases and shortens diagnostic journeys for patients, according to world first study
A world-first scientific study has shown that whole genome sequencing (WGS) can uncover new diagnoses for people across the broadest range of rare diseases investigated to date
Whole genome sequencing improves diagnosis of rare diseases and shortens diagnostic journeys for patients, according to world first study
A world-first scientific study has shown that whole genome sequencing (WGS) can uncover new diagnoses for people across the broadest range of rare diseases investigated to date
Whole genome sequencing improves diagnosis of rare diseases and shortens diagnostic journeys for patients, according to world first study
A world-first scientific study has shown that whole genome sequencing (WGS) can uncover new diagnoses for people across the broadest range of rare diseases investigated to date
Whole Genome Sequencing helps doctors treat Daniel’s rare cancer
Sport-loving schoolboy Daniel is back on the football pitch following precision treatment of a rare kidney tumour
Whole Genome Sequencing helps doctors treat Daniel’s rare cancer
Sport-loving schoolboy Daniel is back on the football pitch following precision treatment of a rare kidney tumour
Whole Genome Sequencing helps doctors treat Daniel’s rare cancer
Sport-loving schoolboy Daniel is back on the football pitch following precision treatment of a rare kidney tumour
Whole Genome Sequencing helps doctors treat Daniel’s rare cancer
Sport-loving schoolboy Daniel is back on the football pitch following precision treatment of a rare kidney tumour
Serena Nik-Zainal wins top prize for ground-breaking research into cancer
Professor Serena Nik-Zainal has been announced as the winner of the 2021 Foulkes Foundation Academy of Medical Sciences Medal
Serena Nik-Zainal wins top prize for ground-breaking research into cancer
Professor Serena Nik-Zainal has been announced as the winner of the 2021 Foulkes Foundation Academy of Medical Sciences Medal
Serena Nik-Zainal wins top prize for ground-breaking research into cancer
Professor Serena Nik-Zainal has been announced as the winner of the 2021 Foulkes Foundation Academy of Medical Sciences Medal
Serena Nik-Zainal wins top prize for ground-breaking research into cancer
Professor Serena Nik-Zainal has been announced as the winner of the 2021 Foulkes Foundation Academy of Medical Sciences Medal