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World’s first gene editing therapy now in the UK for sickle cell diseaseBlogFor many years, treatment options for sickle cell have been limited, focusing mainly on managing symptoms and preventing complications. The approval by NICE of Exa-cel provides new hope for people living with the disease.
AI – doing more with less in the NHSBlogAI and its potential impact on genomics research and clinical practice was peppered throughout this year's Festival of Genomics
Pioneering change: how pharmacogenomics is shaping healthcareBlog Pharmacogenomics - tailoring drug treatments to individuals based on their genetics - is on the cusp of transforming drug prescribing
Support the implementation of emerging health technologies for public benefitNew policy briefing: electrogenetics - a new avenue in precision medicine
Optimise the use of data to deliver better population healthNew policy briefing: electrogenetics - a new avenue in precision medicine
Shape the future of personalised and preventative health servicesA shift in focus to more personalised and preventative approaches to health has the potential to enable people to live healthier lives for longer.
Policy, governance, ethics: refreshing the PHG Foundation’s strategic focusBlogWe want to make science work for health but we also want science that works for health. Here's how.
Data: the catalyst for health and climate action BlogBoth health and climate change are highly complex issues, characterized by numerous interdependencies and multifaceted impacts, making their integration challenging but essential. Chantal Babb de Villiers examines the issues
Metagenomic sequencing in public health – can long read sequencing be used to tackle antimicrobial resistance?BlogLong read sequencing can increase the accuracy when identifying pathogens or presence of drug resistance. This data offers exciting opportunities, especially in the push towards clinical diagnostics and surveillance for antimicrobial resistance.
Optimising EXome PREnatal Sequencing ServicesReportThe optimising EXome PREnatal Sequencing Services (EXPRESS) policy report outlines actions to strengthen clinical implementation of, and further research on, prenatal exome sequencing services in the NHS.