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

Researchers from the Earlham Institute, in collaboration with the Department of Biology at the University of Oxford, have ...

Researchers at the University of California San Diego have identified new genetic variants associated with autism spectrum disorder (ASD) by using long-read whole genome sequencing (LR-WGS), an ...

PacBio’s Revio system and SPRQ-Nx chemistry to enable an order-of-magnitude expansion of HiFi metagenomic sequencing for ...

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

His method of locating genes in human DNA allowed researchers to find disease-causing genes, and later to map the entire, ...

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 ...

An identical twin commits a crime and leaves their DNA at the scene. Can DNA testing reveal which twin is the culprit? This ...

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

A research team led by scientists at the Butantan Institute in São Paulo, Brazil, has completed the most extensive genetic ...

Researchers at Inocras, a bioinformatics-led precision health company harnessing the power of whole-genome sequencing (WGS) ...