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Latest News and Blogs

Automated variant classification workflows in a rare disease laboratory

Automated variant classification workflows in a rare disease laboratory

Helen Savage presented a poster at Rady’s Frontiers in Pediatric Genomic Medicine highlighting the case for automating standardised analysis of cases. 

Congenica assures the clinical safety of NHS genomic analysis

Congenica assures the clinical safety of NHS genomic analysis

Congenica clinical decision support and NGS data analysis provides a complete Clinical Risk Management Process in compliance with the DCB0129 standard

Redressing the balance: Ring Chromosome 20 Syndrome

Redressing the balance: Ring Chromosome 20 Syndrome

Congenica welcomes Allison Watson to talk about her experiences of Ring Chromosome 20 (R(20) - an ultra-rare epilepsy syndrome.

Congenica and Camtech Diagnostics agree strategic partnership to support genomic analysis expansion in Asia

Congenica and Camtech Diagnostics agree strategic partnership to support genomic analysis expansion in Asia

Camtech will market, distribute, sell Congenica rapid NGS data analysis software and clinical decision support in Singapore, Malaysia, Japan, South Korea

Making information about genomic medicine accessible to all 

Making information about genomic medicine accessible to all 

Article by: Alastair Kent OBE FRSA, Chair of the Congenica Patient Advocacy Advisory Board and former Executive Director of Genetic Alliance UK.

Congenica Appoints Jayesh Pankhania as Chief Financial Officer

Congenica Appoints Jayesh Pankhania as Chief Financial Officer

Digital health company Congenica, providing rapid and accurate genomic data analysis software, appoints new Chief Financial Officer, Jayesh Pankhania.

Seeding a Life-Changing International Genomic Insight Alliance to Treat Pediatric Epilepsy

Seeding a Life-Changing International Genomic Insight Alliance to Treat Pediatric Epilepsy

A webinar with experts from Sanford Health and Congenica discussing the applications of genomics to the research and treatment of pediatric epilepsy.

Institute of Immunology and Genetics in Kaiserslautern selects Congenica to accelerate its whole exome sequencing

Institute of Immunology and Genetics in Kaiserslautern selects Congenica to accelerate its whole exome sequencing

Congenica announces a new contract with the Institute of Immunology and Genetics, a leading molecular genetic laboratory in Kaiserslautern, Germany

Why my five-year-old daughter is my inspiration as we fight to understand her sister’s epilepsy

Why my five-year-old daughter is my inspiration as we fight to understand her sister’s epilepsy

March 26 is #Purpleday, an international awareness day that aims to get people talking about epilepsy and raise awareness of the condition. Congenica welcomes guest blogger Adam Clatworthy to tell ...

Sanford Health partners with Congenica to provide answers for undiagnosed rare disease patients

Sanford Health partners with Congenica to provide answers for undiagnosed rare disease patients

Sanford Health selects Congenica clinical decision support platform and NGS data analysis software to provide answers for undiagnosed rare disease patients

Congenica signs distribution agreement with AmpliTech in France

Congenica signs distribution agreement with AmpliTech in France

Congenica, the digital health company enabling rapid and accurate analysis of genomic data, announces a distribution agreement with AmpliTech.   

Congenica Appoints Kamraan Shariff as Chief Business Development Officer

Congenica Appoints Kamraan Shariff as Chief Business Development Officer

Congenica, the company enabling rapid and accurate NGS data analysis to transform lives, today announces the appointment of Kamraan Shariff.