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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.

Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director

Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director

Congenica Ltd, has announced the appointment of Dr Heiner Dreismann as non-executive Director and Senior Independent Director on the board.

Congenica named MedTech Company of the Year 2019

Congenica named MedTech Company of the Year 2019

Congenica has been named MedTech Company of the Year 2019 at the Cambridge Independent Science and Technology Awards 2019 at a ceremony held in Cambridge.

ExomeCG to simplify molecular and cytogenomic data generation and interpretation

ExomeCG to simplify molecular and cytogenomic data generation and interpretation

Nonacus Ltd has announced the launch of ExomeCG, a new product designed by Congenica to simplify the generation and interpretation of molecular and cytogenomic data.

Prenatal exome sequencing in unexplained fetal oedema: a game changer

Prenatal exome sequencing in unexplained fetal oedema: a game changer

Prenatal exome sequencing in unexplained fetal oedema: a game changer

Congenica brings together Mastermind, DECIPHER and Sentieon in major product update

Congenica brings together Mastermind, DECIPHER and Sentieon in major product update

Congenica enables you to achieve 10X faster processing speeds, instantly access genetic evidence and minimize the risk of variants going undetected.

Congenica Integrates Powerful New Curated Data

Congenica Integrates Powerful New Curated Data

Congenica has announced the integration of powerful new reference data sources, DECIPHER and Mastermind® into its clinical decision support platform.

Highlights from the International Conference on Prenatal Diagnosis and Therapy

Highlights from the International Conference on Prenatal Diagnosis and Therapy

Highlights from the International Conference on Prenatal Diagnosis and Therapy