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

Congenica Launches New Host Genetics Module to Advance COVID-19 Research
Congenica's new module accelerates research into the relationship between an individual’s genomic variation & COVID-19 susceptibility & clinical outcomes.

Congenica Express Further Accelerates Identification of Genetic Diseases
Congenica launches an update that will provide automated classification, evidence and reporting of recurrent ‘known’ variants, significantly saving time.

Congenica Prenatal to enable faster research of fetal anomalies in critical prenatal settings
Congenica launches Congenica Prenatal, a new application that facilitate faster, more accurate and comprehensive molecular research into fetal anomalies.

Genomics England Announces New Project to Help in the Fight Against COVID-19
Genomics England has announced a major new sequencing project to uncover how a person’s genetic make-up influences their susceptibility to COVID-19.

Congenica v2.4: Submit and interpret data faster with greater flexibility
With case loads increasing every day, clinical teams are experiencing increasing pressure to make their variant interpretation more efficient.


Whole Genome Sequencing at scale: experiences from a national genome sequencing project
Whole Genome Sequencing at scale: experiences from a national genome sequencing project

RARE Bears bring community together on Rare Disease Day
RARE Bears bring community together on Rare Disease Day

Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders
Congenica today announced the launch of Congenica Neuro, a new application to enable faster analysis of epilepsy and neurodevelopmental disorders.

Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A
Congenica announced the publication of a study on the re-annotation of developmental & epileptic encephalopathy-associated genes with significant clinical implications.

A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder
Congenica platform provides variant review and assessment to support conclusive diagnoses for patients with complex and commonly misdiagnosed bleeding disorders.