In a single experiment, scientists can decipher the entire genomes of many patient samples, animal models, or cultured cells.

Researchers use long-read genome sequencing to discover 33% more structural variants and 38% more tandem repeats linked to autism spectrum disorder.

Element Biosciences created a high-throughput benchtop device that can deliver a whole genome for $100 – half the price of ...

Researchers at the University of California San Diego have identified new genetic variants associated with autism spectrum ...

Routine newborn screening (NBS) has transformed early disease detection. However, traditional biochemical tests limit the ...

Janina Krumbeck, PhD, discusses the clinical advantages of next-generation sequencing over traditional culture and how this ...

Natera NTRA announced the commercial launch of Zenith genomics, a next-generation whole genome sequencing assay designed to ...

A Sydney-based data scientist used AI to create a personalised cancer vaccine for his dog, leading to significant tumour ...

MGI's E25 and G99 sequencers, combined with Predica's Cirnaseq technology and Cirnalyzer software, deliver an affordable and ...

By utilizing long-read sequencing, an emerging technique that reads large sections of the genome at once, scientists at UC San Diego have revealed new genetic variants associated with autism spectrum ...

The tale of this heartbroken tech entrepreneur, his tumour-riddled rescue dog and a cure for cancer has leading scientists ...