The challenge of variant classification

Exploring the complex issue of interpretation - can updated standards and guidelines help achieve increased clarity and consistency? 

Testing toddlers for inherited heart disease

Blood test at birth could reveal genetic high cholesterol levels, potentially preventing heart problems developing in the future

The need for diversity in genomic data

Genomic research calls for broader genetic representation to ensure future healthcare could be truly personalised

The first ‘three-parent baby’ – of many?

Birth of baby boy with DNA from three parents puts ethical debate on mitochondrial transfer technique back in the spotlight

Liquid biopsy – a new era in personalised medicine?

Examining the promises and challenges of exciting advances taking place in genetic testing, aiming to improve diagnosis and reduce patient risk

Personalised medicine in the NHS: what will it mean?

Moving away from trial and error treatments to patient care tailored to your unique genetic makeup  

Nutrigenomics: 5 facts about your genes, diet and health

As nutrigenomics edges nearer to the mainstream, are we any closer to preventing disease through dietary changes?

Gene editing meets gene therapy

Despite continued ethical debate, latest advances in gene editing technologies are poised to transform patient treatment

Examining liquid biopsy in cancer management

Less-invasive method touted as potentially revolutionary for cancer care – could this mean the end for tissue biopsies?

Congenital heart disease study reveals inheritance factor

Examining the genetic roots of cardiac conditions and how further research could bring benefits to patients

Genomics and intellectual disability

Looking into the future of genetic testing for developmental disorders and the promise of genomic insight yet to come 

Genomics and the future of healthcare

Genomics is changing the future of healthcare and medicine - what does this mean for health professionals and their practice?