Latest News and Blogs

Congenica's response to the UK Government's national genomic healthcare strategy, setting out its vision to extend the UK’s leadership in genomics

Supporting Rare Disease Clinical Genomics: The future of genotype phenotype data standards & sharing for analysis to improve medical outcomes

Poster at Rady's Children's Institute Frontiers in Paediatric Medicine Conference discusses the impact of the Deciphering Developmental Disorders study.

Congenica's new module accelerates research into the relationship between an individual’s genomic variation & COVID-19 susceptibility & clinical outcomes.

The future of genomic medicine: can it fulfil its promises?

Dr Charles Steward discusses the role of genomic medicine in investigating rare disease and his own family’s experiences.

Using appropriate reference data sources helps to improve diagnostic yield and can support faster interpretation of genomic data.

Is your laboratory being limited in its ability to scale up its interpretation of genetic data due to the genomic analysis bottleneck?

Experts from Congenica provided commentary on a new report from the World Economic Forum, proposing a new way to share genomic data safely and anonymously.

Looking at the impact of cases receiving molecular diagnosis, it is evident that exome sequencing has significant management implications

How laboratories are reducing the interpretation bottleneck by 95% so that laboratories and national programs can solve more cases.

In this release, we made a significant step on our journey to intelligently, safely, and confidently Automate Variant Classification and reporting.