Congenica v2.4: Submit and interpret data faster with greater flexibility

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New study indicates whole exome sequencing is appropriate for diagnostic testing in both adult and paediatric epilepsy patients

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Faster Genomic Analysis of Neurodevelopmental Disorders with Congenica

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Medical Genetics Awareness Week: exploring the past present and future of medical genetics

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Our Response To Coronavirus COVID-19

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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

Read More

Congenica v2.4: Submit and interpret data faster with greater flexibility

Read More

New study indicates whole exome sequencing is appropriate for diagnostic testing in both adult and paediatric epilepsy patients

Read More

Faster Genomic Analysis of Neurodevelopmental Disorders with Congenica

Read More

Medical Genetics Awareness Week: exploring the past present and future of medical genetics

Read More

Our Response To Coronavirus COVID-19

Read More

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