Login
Please select your location and reference genome:

Latest News and Blogs

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. 

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

Congenica named in UK’s Digital Health Playbook - ‘First 100’ Companies

Congenica named in UK’s Digital Health Playbook - ‘First 100’ Companies

Congenica has been featured in the UK’s Digital Health Playbook ‘First 100’ as one of the UK’s most innovative and impactful digital health companies.   

Genome UK implementation plan

Genome UK implementation plan

Congenica response to Genome UK implementation plan

Dr Charles Steward joins as “friend” of the UK Infantile Spasms Trust

Dr Charles Steward joins as “friend” of the UK Infantile Spasms Trust

Congenica's Dr Charles Steward joins the “friends” of the UK infantile Spasms Trust as an advocate and advisor