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Interview with Seven Bridges: Bill Moss, CEO and Brandi Davis- Dusenbery, CSO tell us what the future holds for Big Data

Data is more than just a hot topic; everyone is focusing on how they can better gather, handle and manipulate […]

Genetics Unzipped Podcast: Involving Patients in Genomics Research

“Nothing about me without me!” is the rallying cry for patient involvement in research. In the latest episode of Genetics […]

Interview with Dr Luigi Grassi, Informatics Scientist, AstraZeneca

I’m Luigi Grassi and I’m an Informatics Scientist at AstraZeneca. I’m responsible for designing and performing bioinformatical analyses of the […]

“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 […]

“We are starting to appreciate non-coding DNA” – Interview with Dr Sandra Smieszek, Vanda Pharmaceuticals Inc.

FLG: Can you introduce yourself and your work? I’m Sandra Smieszek and I’m the Head of Genetics at Vanda Pharmaceuticals […]

Interview with Arianne Shahvisi, Senior Lecturer in Ethics, Brighton and Sussex Medical School

Arianne Shahvisi is a Senior Lecturer in Ethics at the Brighton and Sussex Medical School. We managed to have a chat with Arianne ahead of her speaking at the Festival of Genomics, to get her take on the ‘coloniality’ of health and how the much-hyped advent of Whole Genome Sequencing might play a role in exasperating social injustices.