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

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The Power of a Genetic Diagnosis

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RARE Bears bring community together on Rare Disease Day

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How rapid genomic analysis can improve epilepsy diagnosis and treatment

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

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Re-annotation of Developmental and Epileptic Encephalopathy-associated genes unmasks de novo variants

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Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A

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Maximizing NGS lab efficiency in the analysis and interpretation of genomic data

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A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder

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Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director

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Congenica named MedTech Company of the Year 2019

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

Read More

The Power of a Genetic Diagnosis

Read More

RARE Bears bring community together on Rare Disease Day

Read More

How rapid genomic analysis can improve epilepsy diagnosis and treatment

Read More

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

Read More

Re-annotation of Developmental and Epileptic Encephalopathy-associated genes unmasks de novo variants

Read More

Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A

Read More

Maximizing NGS lab efficiency in the analysis and interpretation of genomic data

Read More

A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder

Read More

Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director

Read More

Congenica named MedTech Company of the Year 2019

Read More