The cause of rare diseases is increasingly being detected through genome sequencing, which involves reading the entire human DNA by first breaking it into small pieces -- short reads. Scientists found ...

Information on tumor mutational status was limited before the development of NGS because traditional Sanger sequencing and ...

Your body is a collection of cells carrying thousands of genetic mistakes accrued over a lifetime—many harmless, some bad and ...

The cause of rare diseases is increasingly being detected through genome sequencing, which involves reading the entire human ...

Archimed, KKR and Novo Holdings are among the PE firms investing in pharma research, development and sales for genetic medicine.

India, a land of vast cultural and genetic diversity, has embarked on an ambitious scientific journey to explore its genetic ...

Scientists have discovered a surprising mechanism by which the inherited genetic mutation known to cause Huntington's disease leads to the death of brain cells. The findings change the understanding ...

New genetic research shows why some people develop deadly Huntington's disease earlier than others. The findings could lead ...

More than 500 European patients with unknown conditions have received a diagnosis through new genetic research.

New research shows that the mutation is, surprisingly, harmless for decades. But it quietly grows into a larger mutation — ...

One area where this evolution is evident is in the coyotes’ diet. Unlike their rural counterparts who primarily feed on rabbits, mice, and other small mammals, urban coyotes tend to have a higher ...