Researchers around world unite to conduct largest study of its kind

Findings counter prevailing ideas about the forces driving genome evolution

Scientists from around the world catalogued 88 million variants

Meet Deep Genomics, a privately-held company that seeks to harness the power of deep learning to transform medicine.

A publication with 940 undergraduate authors demonstrates that research experiences can be offered to far more students than has traditionally been possible

The new experimental assay can help scientists find the precise locations of repair of DNA damage caused by UV radiation and common chemotherapies. The invention could lead to better cancer drugs or improvements in the potency of existing ones.

The switchgrass exhibited mosaic symptoms—splotchy, discolored leaves—characteristic of a viral infection, yet tested negative for known infections. Deep sequencing, a new technology, revealed the plants were infected with a new virus in the genus mastrevirus, the first of its kind found in North America.

A pair of genetics researchers at Iowa State University found striking patterns in the building blocks of DNA in a wide variety of species, according to their recently published paper.

According to the public databases, there are currently approximately 1,900 locations  in the human genome that produce microRNAs (miRNAs), the small and powerful non-coding molecules that regulate numerous cellular processes by reducing the abundance of their targets.  New research published in the Proceedings of the National Academy of Sciences (PNAS) this week adds another roughly 3,400 such locations to that list. Many of the miRNA molecules that are produced from these newly discovered locations are tissue-specific and also human-specific. The finding has big implications for research into how miRNAs drive disease.

Some scientists share better than others. While astronomers and geneticists embrace the concept, the culture of ecology still has a ways to go.