Scientists have identified how specific genetic changes function in cells to influence disease risk and other human health traits. By probing regions of DNA previously linked to disease, the work has ...

Rapidly testing hundreds of thousands of DNA sequences, scientists identified specific genetic variations contributing to blood pressure, cholesterol, and blood sugar.

It seemed deeply unfair that in this era of precision medicine, where targeted therapies are the treatment of choice for ...

New genome sequencing algorithm boosts human genome completeness by 20%, improving variant detection and advancing personalized medicine.

A study from an international team of experts in veterinary medicine, human medicine and genomics provides the first ...

Law enforcement said they're considering using genetic genealogy to test the DNA found at the Arizona home of Nancy Guthrie.

Researchers used genomic structural equation modeling to separate schizophrenia-specific and shared bipolar genetic risks. Schizophrenia-unique variants were linked to lower IQ, while shared variants ...

For decades, scientists viewed the genome of a newly fertilised egg as a structural 'blank slate' – a disordered tangle of ...

For many years, researchers believed that the DNA inside a newly fertilized egg began as a structural ‘blank slate’ – a loose ...

TruPath™ Genome offers more complete genome, with the simplest sample to sequencer workflowData presented at AGBT ...

The expert anglers at Milliken Fishing use Google Maps in a new way to locate urban culverts full of unsuspecting bass.

A massive genomics effort has identified thousands of single nucleotide non-coding variants, which alter gene activity, that link to disease and health.