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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
Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director
Posted 5th November 2019

Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director

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News , Investor
Congenica named MedTech Company of the Year 2019
Posted 1st November 2019

Congenica named MedTech Company of the Year 2019

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News
ExomeCG to simplify molecular and cytogenomic data generation and interpretation
Posted 17th October 2019

ExomeCG to simplify molecular and cytogenomic data generation and interpretation

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News
Prenatal exome sequencing in unexplained fetal oedema: a game changer
Posted 16th October 2019

Prenatal exome sequencing in unexplained fetal oedema: a game changer

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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

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
News
Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director
Posted November Nov 5th 2019

Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director

Read More
News , Investor
Congenica named MedTech Company of the Year 2019
Posted November Nov 1st 2019

Congenica named MedTech Company of the Year 2019

Read More
News
ExomeCG to simplify molecular and cytogenomic data generation and interpretation
Posted October Oct 17th 2019

ExomeCG to simplify molecular and cytogenomic data generation and interpretation

Read More
News
Prenatal exome sequencing in unexplained fetal oedema: a game changer
Posted October Oct 16th 2019

Prenatal exome sequencing in unexplained fetal oedema: a game changer

Read More
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