Recent Posts

Blog, precision medicine, geneticdiagnosis
Best practices in automatable clinical decision support workflows
Posted 7th December 2021

Best practices in automatable clinical decision support workflows

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Blog , Patient Advocacy , genomics
Whole Genome Sequencing at Birth: What Should Be Looked For?
Posted 25th November 2021

Whole Genome Sequencing at Birth: What Should Be Looked For?

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Blog , genomics , precision medicine
​Why choose a professional solution for your genomic data analysis?
Posted 24th November 2021

​Why choose a professional solution for your genomic data analysis?

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Patient Advocacy , RareDiseases , VAMP2
A Ray of Sunshine
Posted 18th November 2021

A Ray of Sunshine

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Blog , NGS , GRCh38
Making the jump from GRCh37 to GRCh38
Posted 12th November 2021

Making the jump from GRCh37 to GRCh38

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Blog , Patient Advocacy , genomics , RareDiseases
Opening the Black Box: Telling the Story of a Genomic Diagnosis
Posted 11th November 2021

Opening the Black Box: Telling the Story of a Genomic Diagnosis

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News , RareDiseases , GenomicsEngland
Congenica named as genomic analysis platform in ‘Impact of the 100,000 Genomes Pilot – Preliminary Report’ in the New England Journal of Medicine
Posted 11th November 2021

Congenica named as genomic analysis platform in ‘Impact of the 100,000 Genomes Pilot – Preliminary Report’ in the New England Journal of Medicine

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Blog , genomics , RareDiseases , GenomicsEngland
100k Genomes Pilot on Rare Disease Diagnosis in Healthcare
Posted 11th November 2021

100k Genomes Pilot on Rare Disease Diagnosis in Healthcare

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Congenica’s commitment to quality - World Quality Week 2021
Posted 9th November 2021

Congenica’s commitment to quality - World Quality Week 2021

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Blog , epilepsy
Nick Lench is appointed as Trustee of Epilepsy Research UK
Posted 5th November 2021

Nick Lench is appointed as Trustee of Epilepsy Research UK

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Blog , EVENT
Automation and AI improve driving improvements in genomic testing
Posted 4th November 2021

Automation and AI improve driving improvements in genomic testing

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1 2 3 4 5
... 19 next
Blog , precision medicine , geneticdiagnosis
Best practices in automatable clinical decision support workflows
Posted 7th December 2021

Best practices in automatable clinical decision support workflows

Read More
Blog , Patient Advocacy , genomics
Whole Genome Sequencing at Birth: What Should Be Looked For?
Posted November Nov 25th 2021

Whole Genome Sequencing at Birth: What Should Be Looked For?

Read More
Blog , genomics , precision medicine
​Why choose a professional solution for your genomic data analysis?
Posted November Nov 24th 2021

​Why choose a professional solution for your genomic data analysis?

Read More
Patient Advocacy , RareDiseases , VAMP2
A Ray of Sunshine
Posted November Nov 18th 2021

A Ray of Sunshine

Read More
Blog , NGS , GRCh38
Making the jump from GRCh37 to GRCh38
Posted November Nov 12th 2021

Making the jump from GRCh37 to GRCh38

Read More
Blog , Patient Advocacy , genomics , RareDiseases
Opening the Black Box: Telling the Story of a Genomic Diagnosis
Posted November Nov 11th 2021

Opening the Black Box: Telling the Story of a Genomic Diagnosis

Read More
News , RareDiseases , GenomicsEngland
Congenica named as genomic analysis platform in ‘Impact of the 100,000 Genomes Pilot – Preliminary Report’ in the New England Journal of Medicine
Posted November Nov 11th 2021

Congenica named as genomic analysis platform in ‘Impact of the 100,000 Genomes Pilot – Preliminary Report’ in the New England Journal of Medicine

Read More
Blog , genomics , RareDiseases , GenomicsEngland
100k Genomes Pilot on Rare Disease Diagnosis in Healthcare
Posted November Nov 11th 2021

100k Genomes Pilot on Rare Disease Diagnosis in Healthcare

Read More
Congenica’s commitment to quality - World Quality Week 2021
Posted November Nov 9th 2021

Congenica’s commitment to quality - World Quality Week 2021

Read More
Blog , epilepsy
Nick Lench is appointed as Trustee of Epilepsy Research UK
Posted November Nov 5th 2021

Nick Lench is appointed as Trustee of Epilepsy Research UK

Read More
Blog , EVENT
Automation and AI improve driving improvements in genomic testing
Posted November Nov 4th 2021

Automation and AI improve driving improvements in genomic testing

Read More
1 2 3 4 5
... 19 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.