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Recent Posts
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News
Blog
News
Posted 17th March 2020
Whole Genome Sequencing at scale: experiences from a national genome sequencing project
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Blog
Posted 3rd March 2020
The Power of a Genetic Diagnosis
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News
Posted 28th February 2020
RARE Bears bring community together on Rare Disease Day
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Blog
Posted 28th January 2020
How rapid genomic analysis can improve epilepsy diagnosis and treatment
Read More
News
,
Investor
,
Product
Posted 14th January 2020
Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders
Read More
Blog
Posted 5th December 2019
Re-annotation of Developmental and Epileptic Encephalopathy-associated genes unmasks de novo variants
Read More
News
Posted 3rd December 2019
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A
Read More
Blog
Posted 2nd December 2019
Maximizing NGS lab efficiency in the analysis and interpretation of genomic data
Read More
News
Posted 12th November 2019
A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder
Read More
News
Posted 5th November 2019
Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director
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News
,
Investor
Posted 1st November 2019
Congenica named MedTech Company of the Year 2019
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News
Posted 17th March 2020
Whole Genome Sequencing at scale: experiences from a national genome sequencing project
Read More
Blog
Posted March Mar 3rd 2020
The Power of a Genetic Diagnosis
Read More
News
Posted February Feb 28th 2020
RARE Bears bring community together on Rare Disease Day
Read More
Blog
Posted January Jan 28th 2020
How rapid genomic analysis can improve epilepsy diagnosis and treatment
Read More
News
,
Investor
,
Product
Posted January Jan 14th 2020
Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders
Read More
Blog
Posted December Dec 5th 2019
Re-annotation of Developmental and Epileptic Encephalopathy-associated genes unmasks de novo variants
Read More
News
Posted December Dec 3rd 2019
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A
Read More
Blog
Posted December Dec 2nd 2019
Maximizing NGS lab efficiency in the analysis and interpretation of genomic data
Read More
News
Posted November Nov 12th 2019
A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder
Read More
News
Posted November Nov 5th 2019
Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director
Read More
News
,
Investor
Posted November Nov 1st 2019
Congenica named MedTech Company of the Year 2019
Read More
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