Recent Posts

Blog, Patient Advocacy, RareDiseases, Schinzel-Giedion Syndrome, Chapter 1
How Schinzel-Giedion Syndrome (SGS) has changed our lives
Posted 28th May 2021

How Schinzel-Giedion Syndrome (SGS) has changed our lives

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News , genomics
Congenica named in UK’s Digital Health Playbook - ‘First 100’ Companies
Posted 27th May 2021

Congenica named in UK’s Digital Health Playbook - ‘First 100’ Companies

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News , genomics
Genome UK implementation plan
Posted 24th May 2021

Genome UK implementation plan

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Blog , Patient Advocacy , epilepsy , RareDiseases , Chapter 8
Dr Charles Steward joins as “friend” of the UK Infantile Spasms Trust
Posted 21st May 2021

Dr Charles Steward joins as “friend” of the UK Infantile Spasms Trust

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Blog , poster , prenatal , INGENIOUS , NGS
Improved Next Generation Sequencing for Ultrasound Abnormalities (INGENIOUS)
Posted 17th May 2021

Improved Next Generation Sequencing for Ultrasound Abnormalities (INGENIOUS)

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Blog , Patient Advocacy , Champ1 , RareDiseases
Our CHAMP1 journey
Posted 14th May 2021

Our CHAMP1 journey

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News , Product
Congenica 3.1 - Automating best practices in variant interpretation
Posted 12th May 2021

Congenica 3.1 - Automating best practices in variant interpretation

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Blog , Patient Advocacy , cerebral palsy
Dr Charles Steward elected to the ICPGC GC
Posted 11th May 2021

Dr Charles Steward elected to the ICPGC GC

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Blog , Patient Advocacy , genomics , SCN8A , Chapter 1
SCN8A – the needle in the haystack 
Posted 30th April 2021

SCN8A – the needle in the haystack 

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Blog , Clinical Cases , genomics
Exome analysis of cases with skeletal dysplasia
Posted 28th April 2021

Exome analysis of cases with skeletal dysplasia

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Blog , Clinical Cases , genomics
Automated variant classification workflows in a rare disease laboratory
Posted 28th April 2021

Automated variant classification workflows in a rare disease laboratory

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Blog , Patient Advocacy , RareDiseases , Schinzel-Giedion Syndrome , Chapter 1
How Schinzel-Giedion Syndrome (SGS) has changed our lives
Posted 28th May 2021

How Schinzel-Giedion Syndrome (SGS) has changed our lives

Read More
News , genomics
Congenica named in UK’s Digital Health Playbook - ‘First 100’ Companies
Posted May May 27th 2021

Congenica named in UK’s Digital Health Playbook - ‘First 100’ Companies

Read More
News , genomics
Genome UK implementation plan
Posted May May 24th 2021

Genome UK implementation plan

Read More
Blog , Patient Advocacy , epilepsy , RareDiseases , Chapter 8
Dr Charles Steward joins as “friend” of the UK Infantile Spasms Trust
Posted May May 21st 2021

Dr Charles Steward joins as “friend” of the UK Infantile Spasms Trust

Read More
Blog , poster , prenatal , INGENIOUS , NGS
Improved Next Generation Sequencing for Ultrasound Abnormalities (INGENIOUS)
Posted May May 17th 2021

Improved Next Generation Sequencing for Ultrasound Abnormalities (INGENIOUS)

Read More
Blog , Patient Advocacy , Champ1 , RareDiseases
Our CHAMP1 journey
Posted May May 14th 2021

Our CHAMP1 journey

Read More
News , Product
Congenica 3.1 - Automating best practices in variant interpretation
Posted May May 12th 2021

Congenica 3.1 - Automating best practices in variant interpretation

Read More
Blog , Patient Advocacy , cerebral palsy
Dr Charles Steward elected to the ICPGC GC
Posted May May 11th 2021

Dr Charles Steward elected to the ICPGC GC

Read More
Blog , Patient Advocacy , genomics , SCN8A , Chapter 1
SCN8A – the needle in the haystack 
Posted April Apr 30th 2021

SCN8A – the needle in the haystack 

Read More
Blog , Clinical Cases , genomics
Exome analysis of cases with skeletal dysplasia
Posted April Apr 28th 2021

Exome analysis of cases with skeletal dysplasia

Read More
Blog , Clinical Cases , genomics
Automated variant classification workflows in a rare disease laboratory
Posted April Apr 28th 2021

Automated variant classification workflows in a rare disease laboratory

Read More
previous 1 ...
6 7 8 9 10
... 22 next
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