A collaborative study from the MRC Laboratory of Medical Sciences (LMS) and Imperial College London has found that the ...

New study links childhood maltreatment to genetic changes and higher risks of schizophrenia, ADHD, and depression, ...

Artificial intelligence is rapidly becoming medicine’s most powerful microscope, revealing patterns in human DNA that were ...

Genetic ancestry is a concept that has long captured people’s imaginations. It’s no surprise that it’s been turned into a ...

Parse Biosciences, the leading provider of scalable and accessible single cell sequencing solutions, today announced a collaboration with Codebreaker Labs to develop and validate a breakthrough ...

Reliance Industries is planning to enter another market-disrupting sector by offering genomic diagnostic tests at prices below Rs 1,000, a steep reduction from the current basic rates of around Rs ...

Nabsys 2.0, LLC (Nabsys), a pioneer in electronic genome mapping technology, in partnership with Hitachi High-Tech ...

Singlera Genomics, a company focused on the application of novel DNA methylation technologies to genetic diagnosis, with ...

The largest study so far into the genetics of chronic fatigue syndrome, or myalgic encephalomyelitis, has implicated 259 ...

Singlera Genomics, a company focused on the application of novel DNA methylation technologies to genetic diagnosis, with their partner Breakthrough Genomics, ...

Over the past decades, large-scale human genetic studies have identified numerous risk genes and variants associated with complex diseases and traits.

A research team led by the Department of Pediatrics and Adolescent Medicine, School of Clinical Medicine, LKS Faculty of ...