Insights into Rare Disease from the Congenica Team
We work to improve the lives of people living with rare and inherited diseases. Here, some of our team talk about what rare disease means to them.
From Lung Collapse to Ironman
Lea has BHD and shares her empowering story with us for Rare Disease Day. See Lea's inspirational journey from lung collapse to Ironman in this video.
The Impact of NHS Genomics Medicine Service on Rare Disease
A new film about the NHS Genomic Medicine Service and how it is benefiting those affected by rare diseases in the UK, both today and in the future.
Hopes for the future of Precision Medicine
Professor Philip Beales, Professor Sarah Weckhuysen, and Professor Jozef Gocz discuss the future of precision medicine and answer commonly asked questions.
Congenica AI at Festival of Genomics
Watch our presentation from Festival of Genomics 'Fully Interpretable AI-Driven Variant Prioritization Delivers Fast, Actionable Results for Patients'.
Celebrating Congenica's Women in Science
On International Day of Woman and Girls in Science we celebrate the role that women at Congenica play in science and technology.
Congenica 3.3 improves genomic data analysis and automates workflow
Congenica v3.3 uses Congenica’s AI combined with other platform features to further improve genomic data analysis and automate workflow.
Global barriers to genomics - Malaysian Epilepsy Conference
A look at the barriers to genomics around the world, starting with a webinar in Malaysia, ‘Epilepsy Advocacy: Challenges and Opportunities’.
Added fear of mortality for rare caregivers
Being a parent to a rare child is hard enough day to day. What happens when one of the parents is diagnosed with a potentially life-threatening disorder?
Enabling Genomic Medicine in China
On Wednesday 15 December, Congenica held its virtual Enabling Genomic Medicine 2021 China event. all sessions from the event are now available on demand.
Bringing genomics into the heart of healthcare
Christina Waters, SVP of Global Genomic Insights and Solutions, asks why aren't there better disease therapies out there?
Full Speed Ahead for FAM177A1: Two Siblings' Diagnostic Odyssey
Jill Hawkins is founder and president of Fam177A1. an organization she set up following the diagnosis that two of her children have large deletions on their FAM177A1 gene. Here she tells her story.