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An impact study on the rare disease community: a call to action

Jo Balfour, one of the founding members and current Operations Manager at Cambridge Rare Disease Network (CRDN), has collaborated with […]

The impact of COVID-19 on the rare disease community

For the last few weeks, we have been covering COVID-related stories, from the sequencing of the virus, the research efforts, […]

“Usually, you’re relatively alone in your rare disease community” – Interview with Shelley Simmonds, Patient Advocate for rare diseases

Shelley Simmonds is a patient advocate whose son has Duchenne muscular dystrophy. Duchenne causes muscle weakening and wasting and is […]

World of Genomics: Estonia

‘World of Genomics: Estonia’ – Original article written by Shannon Gunn, 2021. Updated by Lyndsey Fletcher, April 2024. For the […]

The Festival of Genomics & Biodata Boston 2024 

Are you ready? The Festival of Genomics & Biodata is heading back to Boston!  After a triumphant return to the […]

Diversity in Genomics: Assessing the Mosaic of Human Life

Despite our DNA only differing at around 0.1% of base pairs, human life is complex, unique and varied. Although this […]

World of Genomics: The Philippines

In this week’s World of Genomics, we explore the Philippines, an archipelago in Southeast Asia famous for its stunning natural […]

World of Genomics: Belgium

Original article written by Anjum Aktar, November 2022. Updated by Aleisha Collins, January 2024. Nestled in the heart of Europe, […]

Clinical Trials – What is holding liquid biopsy back?

This feature is written using content from our recently published Liquid Biopsy report, which you can read in full by […]

Liquid Biopsy Report – A New Era in Disease Detection and Surveillance

Liquid biopsy is poised to redefine the way we approach diagnostics and personalized medicine in the treatment of complex diseases. […]