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News, Investor, Product
Congenica Launches New Host Genetics Module to Advance COVID-19 Research
Posted 22nd September 2020

Congenica Launches New Host Genetics Module to Advance COVID-19 Research

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News , Investor , Product
Congenica Express Further Accelerates Identification of Genetic Diseases
Posted 15th July 2020

Congenica Express Further Accelerates Identification of Genetic Diseases

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News , Investor , Product
Congenica Prenatal to enable faster research of fetal anomalies in critical prenatal settings
Posted 4th June 2020

Congenica Prenatal to enable faster research of fetal anomalies in critical prenatal settings

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News , Investor
Genomics England Announces New Project to Help in the Fight Against COVID-19
Posted 13th May 2020

Genomics England Announces New Project to Help in the Fight Against COVID-19

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News , Investor , Product
Congenica v2.4: Submit and interpret data faster with greater flexibility
Posted 29th April 2020

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

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News
Our Response To Coronavirus COVID-19
Posted 23rd March 2020

Our Response To Coronavirus COVID-19

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News
Whole Genome Sequencing at scale: experiences from a national genome sequencing project
Posted 17th March 2020

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

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News
RARE Bears bring community together on Rare Disease Day
Posted 28th February 2020

RARE Bears bring community together on Rare Disease Day

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News , Investor , Product
Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders
Posted 14th January 2020

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

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News
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A
Posted 3rd December 2019

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

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News
A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder
Posted 12th November 2019

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

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News , Investor , Product
Congenica Launches New Host Genetics Module to Advance COVID-19 Research
Posted 22nd September 2020

Congenica Launches New Host Genetics Module to Advance COVID-19 Research

Read More
News , Investor , Product
Congenica Express Further Accelerates Identification of Genetic Diseases
Posted July Jul 15th 2020

Congenica Express Further Accelerates Identification of Genetic Diseases

Read More
News , Investor , Product
Congenica Prenatal to enable faster research of fetal anomalies in critical prenatal settings
Posted June Jun 4th 2020

Congenica Prenatal to enable faster research of fetal anomalies in critical prenatal settings

Read More
News , Investor
Genomics England Announces New Project to Help in the Fight Against COVID-19
Posted May May 13th 2020

Genomics England Announces New Project to Help in the Fight Against COVID-19

Read More
News , Investor , Product
Congenica v2.4: Submit and interpret data faster with greater flexibility
Posted April Apr 29th 2020

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

Read More
News
Our Response To Coronavirus COVID-19
Posted March Mar 23rd 2020

Our Response To Coronavirus COVID-19

Read More
News
Whole Genome Sequencing at scale: experiences from a national genome sequencing project
Posted March Mar 17th 2020

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

Read More
News
RARE Bears bring community together on Rare Disease Day
Posted February Feb 28th 2020

RARE Bears bring community together on Rare Disease Day

Read More
News , Investor , Product
Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders
Posted January Jan 14th 2020

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

Read More
News
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A
Posted December Dec 3rd 2019

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

Read More
News
A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder
Posted November Nov 12th 2019

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

Read More
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... 11 next
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