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Latest News and Blogs

Genome UK: the future of healthcare

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 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 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 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 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

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.

Our Response To Coronavirus COVID-19

Our Response To Coronavirus COVID-19

Our Response To Coronavirus COVID-19 - Congenica

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

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

RARE Bears bring community together on Rare Disease Day

Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders

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

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

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.