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 ...

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

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

Nucleic acid therapies offer targeted treatment for genetic diseases, but delivery remains a key hurdle. Explore how advances ...

Mammalian cells are tricky evolution hosts. They grow slowly, contain large genomes, and regulate protein behavior through ...

New research suggests that DNA sequences historically considered to be "junk" have had an overlooked role in gene expression this whole time.

Single-cell RNA sequencing of thousands of yeast progeny reveals how gene expression differences and heritability drive phenotypic diversity.

In a giant feat of genetic engineering, scientists have created bacteria that make proteins in a radically different way than ...