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Latest News and Blogs

Rapid diagnosis of Long QT syndrome protects family from major health risk

Rapid diagnosis of Long QT syndrome protects family from major health risk

Congenica supports the rapid diagnosis of Long QT syndrome and enables consideration of potentially life-saving interventions for baby and mother.

Clinical OMICs interview with David Atkins CEO Congenica

Clinical OMICs interview with David Atkins CEO Congenica

Clinical OMICs features an interview with Congenica CEO David Atkins who talks about the genomic medicine landscape and Congenica's plans for the future.

Raising awareness of Dravet Syndrome

Raising awareness of Dravet Syndrome

Galia Wilson and Claire Eldred have provided us with today's article in recognition of International Dravet Syndrome Awareness day, Wednesday 23rd June. 

Genomics in the Clinic & the Promise of Precision Medicine

Genomics in the Clinic & the Promise of Precision Medicine

At PMLS Precision Medicine and Rare Disease event, Congenica took part in a panel entitled 'Genomics in the Clinic and the Promise of Precision Medicine'.

Our story of Norrie Disease

Our story of Norrie Disease

We welcome guest blogger Carla Golledge, who shares her story about son Cameron who was born with Norrie disease. 

Congenica funded to reduce fatal drug interactions by mapping genes

Congenica funded to reduce fatal drug interactions by mapping genes

New software to reduce the number of adverse drug reactions is being developed thanks to a joint investment of £2 million provided by UKRI and L& G.

The challenges and opportunities for growth during a global pandemic

The challenges and opportunities for growth during a global pandemic

Congenica's Chairman Andy Richards and CEO David Atkins join leaders from biotech / pharma sector to discuss the impact of pandemic in the last 18 months.

Enhanced whole exome analysis enables Veritas Intercontinental to solve more cases

Enhanced whole exome analysis enables Veritas Intercontinental to solve more cases

Veritas Genetics partnered with Congenica to improve diagnostic yield & increase the efficiency, throughput and speed of analysis in diagnostic laboratory

Genomic sequencing in a prenatal setting - posters presented at ISPD

Genomic sequencing in a prenatal setting - posters presented at ISPD

Two members of Congenica’s Clinical Interpretation Services team presented posters at the International Conference on Prenatal Diagnosis and Therapy (ISPD)

Mutual Collaboration focus for CRDN Companies Forum

Mutual Collaboration focus for CRDN Companies Forum

Alastair Kent and Dr Charles Steward attended the virtual Cambridge Rare Disease Network (CRDN) Companies Forum Patient Group and Industry Partnering event

Helping to Further the Patient Impact of Genomics

Helping to Further the Patient Impact of Genomics

Dr Charles Steward was interviewed for podcast, Once Upon a Gene, where Effie speaks to others about their journey through life with rare disease.

How Schinzel-Giedion Syndrome (SGS) has changed our lives

How Schinzel-Giedion Syndrome (SGS) has changed our lives

Nuala Summerfield tells the story of her daughter's diagnosis of rare disease Schinzel-Giedion Syndrome (SGS) and setting up The SGS Foundation