A breakthrough NHS study reveals whole-genome sequencing provides diagnoses for rare genetic conditions two years earlier, offering families crucial answers and access to care. Read the inspiring story of three-year-old Nathaniel.
A breakthrough NHS study reveals whole genome sequencing is diagnosing rare genetic conditions in children two years sooner, transforming care for families like Nathaniel's in London.
A landmark NHS study reveals whole genome sequencing is diagnosing rare genetic conditions in children two years earlier, transforming care for families like three-year-old Nathaniel's.
Scientists have sequenced the massive genome of the deep-sea vampire squid, offering unprecedented insights into how octopuses and squids evolved from a common ancestor over 300 million years ago.
Cambridge scientists achieve unprecedented DNA mapping milestone that could revolutionise medicine and transform our understanding of genetic diseases
Groundbreaking research reveals humans are evolving in ways never seen before, with natural selection actively shaping our genomes and removing harmful mutations at an accelerating pace.
Oxford University researchers are pioneering a groundbreaking NHS initiative that could bring DNA sequencing to GP surgeries, transforming preventative healthcare and early disease detection across the UK.
Groundbreaking genetic research brings the dream of resurrecting the extinct dodo bird one step closer to reality. Scientists achieve a major milestone in sequencing its genome, sparking both excitement and ethical debate.