Blog

Researcher Holly Ellard explores written communication in the Genomic Medicine Service by looking at letters to patients.

Researcher Alfredo Dueñas Rey shares how data from the National Genomic Research Library helped him to find genetic causes of rare inherited eye conditions.

Eva Medico Salsench shares how whole genome sequencing helped her genetically diagnose patients with hereditary spastic paraplegia.

Sunandini Ramnarayanan shares how the National Genomic Research Library is supporting her to understand the role of 'DNA dark matter' in cancer.

An early career researcher in our research community shares her latest work with machine learning and radiogenomics and what's next for her.

An early career researcher in our research community shares his latest work and what's coming next for him.