Recent Posts

Blog, case study
Enhanced whole exome analysis enables Veritas Intercontinental to solve more cases
Posted 15th June 2021

Enhanced whole exome analysis enables Veritas Intercontinental to solve more cases

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Clinical Cases , prenatal , EVENT , posters
Genomic sequencing in a prenatal setting - posters presented at ISPD
Posted 14th June 2021

Genomic sequencing in a prenatal setting - posters presented at ISPD

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Blog , Patient Advocacy
Mutual Collaboration focus for CRDN Companies Forum
Posted 11th June 2021

Mutual Collaboration focus for CRDN Companies Forum

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Blog , Patient Advocacy , epilepsy , cerebral palsy
Helping to Further the Patient Impact of Genomics
Posted 4th June 2021

Helping to Further the Patient Impact of Genomics

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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

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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 , case study
Enhanced whole exome analysis enables Veritas Intercontinental to solve more cases
Posted 15th June 2021

Enhanced whole exome analysis enables Veritas Intercontinental to solve more cases

Read More
Clinical Cases , prenatal , EVENT , posters
Genomic sequencing in a prenatal setting - posters presented at ISPD
Posted June Jun 14th 2021

Genomic sequencing in a prenatal setting - posters presented at ISPD

Read More
Blog , Patient Advocacy
Mutual Collaboration focus for CRDN Companies Forum
Posted June Jun 11th 2021

Mutual Collaboration focus for CRDN Companies Forum

Read More
Blog , Patient Advocacy , epilepsy , cerebral palsy
Helping to Further the Patient Impact of Genomics
Posted June Jun 4th 2021

Helping to Further the Patient Impact of Genomics

Read More
Blog , Patient Advocacy , RareDiseases , Schinzel-Giedion Syndrome , Chapter 1
How Schinzel-Giedion Syndrome (SGS) has changed our lives
Posted May May 28th 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
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... 18 next
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Congenica is available as a CE Marked IVD clinical decision support platform for clinical diagnostic use for inherited genetic disorders in the UK and EU, Iceland, Lichtenstein, Norway, Switzerland and Turkey. In all other countries, ensuring compliance with relevant local, national and international clinical laboratory regulations is the responsibility of the laboratory.