Recent Episodes...

See how tools like long read sequencing, RNA sequencing, MAVEs, and AI are ethically transforming WGS to make patients lives better.

Baylor Genetics’ Chief Medical Officer Dr. Christine Eng explains how RNA sequencing complements DNA testing to unlock diagnoses for rare disease patients.

How whole genome sequencing is transforming rare disease diagnosis in Brazil featuring MGI’s Victor Camillo and Neogenomica’s Dr. João Bosco Oliveira.

Listen to The Persistence Lab, a new podcast from AbbVie. Hosted by Kira Dineen, the series explores how scientists, patients, and experts look to solve some of the toughest challenges in medicine and health care, one step at a time.

Recorded live at Connecticut’s Darwin Day Event, we examine natural selection, horizontal gene transfer, and how Charles Darwin’s ideas continue to shape genomic science.

Michele Magner explains how genetics can prevent medication harm in older adults, so people can successfully age in place.

Clinical geneticist Dr. Amy Kritzer reveals why Fabry disease looks so different across sexes and what that means for diagnosis and treatment.

Drs. Yuming Hu and Elizabeth Bhoj on bridging research and real-world impact through scientific publishing.

From early chemotherapy response testing to AI-driven precision medicine, the host of Genetics for Healthcare Rome Madison, shares the evolving eras of genetic testing.

Kristin McKay, Executive Director of Project Alive, is dedicated to accelerating treatments, expanding care, and supporting families affected by Hunter Syndrome, a disease that impacted her brother and now her son.