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Embedding genomics in the UK health systemCase studyThe 2020 Clinical genome analysis evidence review from PHG Foundation fed directly into strategic planning for the design and provision of clinical genetic services in Scotland
Long read technologies – the next frontier of clinical genome sequencing?BlogAs genomic medicine becomes further established in the NHS, a new generation of sequencers capable of reading exceptionally long stretches of DNA is causing a stir in genomics research.
Improving risk prediction for cancerCase studyOur 2014 report, Stratified Screening for Cancer urges policy and decision makers to prepare for the introduction of risk-stratified screening for breast and prostate cancers.
Next steps in the sequenceCase studyThe 2020 Clinical genome analysis evidence review from PHG Foundation fed directly into strategic planning for the design and provision of clinical genetic services in Scotland
The NHS App, good for patients, good for the NHS?BlogJeremy Hunt challenged NHS Digital to deliver access to eight digital services through a single patient app by the end of 2018.
Preparing for clinical genome sequencingCase studyThe PHG Foundation continues to advocate, inform and support the development of policy on genomics and 'omics technologies in clinical and public health services.
Prevention gaining ground in the battle against breast cancerBlogHow can health systems support populations and individuals to understand and reduce breast cancer risk?
The role of citizen generated data for healthBlogOver the past few months PHG Foundation has been exploring the role of citizen generated data in health by looking at themes such as patient participation in their care and the increasingly blurred line between lifestyle and medical devices
Meet the expert – Fiona AdsheadBlogIn our first meet the expert blog, Fiona Adshead talks to us about wellbeing, person centred healthcare and what’s currently happening in the health clinic