A new genetic screening method allows researchers to efficiently modulate individual genes across entire tissues and provides ...

A U.S. bankruptcy judge on Tuesday approved a $46.75 ​million settlement for victims of a 2023 data breach at ‌the genetic ...

Sample pooling, in which equal volumes from multiple specimens are combined and tested together, can reduce per-sample costs and increase testing throughput while preserving clinical performance.

UCSF researchers are using tiny "mini-organs" to model disease, personalize treatment, and understand human development. They ...

Researchers from the Cancer Science Institute of Singapore (CSI Singapore) at NUS have developed a new method that allows ...

Some IVF clinics are using AI to perform tasks such as sperm and embryo selection, but some fertility experts question ...

Bionano Genomics, Inc. (Nasdaq: BNGO) today announced that studies featuring optical genome mapping (OGM) at the 2026 European Society of Human Genetics (ESHG) conference grew substantially compared ...

Congenital heart disease (CHD) is the most common birth defect and a leading cause of infant mortality. CHD often has a genetic cause, and recent studies demonstrate the utility of genetic testing. In ...

Daniel Combs, MD, is an Assistant Professor of Pediatrics and Medicine at the University of Arizona. Clinical signs raise suspicion for Prader-Willi syndrome (PWS), but genetic testing confirms it.

After a decade of clinical assessments failed to meet DSM-5 criteria, a chromosomal microarray revealed the genetic truth behind a complex neurodevelopmental presentation. This question addresses a ...