Routine newborn screening (NBS) has transformed early disease detection. However, traditional biochemical tests limit the range of conditions that can be identified at birth. Next-generation ...

A genomic test developed at UC San Francisco to rapidly detect almost any kind of pathogen – virus, bacteria, fungus or parasite – has proved successful after a decade of use. The test has the ...

This voice experience is generated by AI. Learn more. This voice experience is generated by AI. Learn more. Whole-genome sequencing in routine care is now solving rare disease cases at scale, with ...

A phase II study of pevonedistat in combination with carboplatin and paclitaxel in advanced intrahepatic cholangiocarcinoma: ECOG-ACRIN EA2187. Real-world validation of the risk estimation of tumor ...

More than a decade ago, researchers launched the BabySeq Project, a pilot program to return newborn genomic sequencing results to parents and measure the effects on newborn care. Today, over 30 ...

The Translational Genomics Research Institute (TGen), part of City of Hope, today announced the launch of JAYseqTM, a ...

Michigan Tech's Genomic Sequencing Lab, part of the University's Health Research Institute, plays a leading role in tracking animal-borne illnesses in the Upper Peninsula region while also advancing ...

Driving community impact Providence integrates precision medicine to improve cancer care and close clinical quality gaps across its health system.

A routine experiment with a new single-cell DNA sequencing method turned into a surprising scientific twist when researchers ...