Scientists used diverse genomes to complete a fuller human DNA map. This unlocks hidden risks and improves diagnoses.

We spoke with Neil Ward from PacBio about England’s plan to introduce whole genome sequencing for every newborn, and how long-read technology is shaping the future of early diagnosis around the world.

We may be on the cusp of a new era of biochemical discovery, but turning these advancements into drugs isn’t so easy ...

His genome held strange secrets: a turbocharged alcohol gene, rewired brain chemistry, and a slow-burn caffeine receptor.

New research from the Perelman School of Medicine at the University of Pennsylvania has challenged the belief that the likelihood of finding undiagnosed genetic conditions decreases with age. “Our ...

Researchers at the Hebrew University of Jerusalem have successfully revived fungal specimens collected over 80 years ago, ...

According to a new comprehensive report from The Insight Partners, the global mRNA sequencing market is observing ...

Neurodegenerative diseases are chronic conditions that cause nerve cells to lose function and die over many years. A decade-long, gradual mental decline often precedes this ultimately fatal process.

To lead in this era, medtech companies must expand how they innovate — combining scientific rigor with human connection, ...

For this week's Pulse Check, I connected with Robert Stone, CEO of City of Hope, one of the nation's largest cancer research ...