Omics

Ki67 in healthy breast tissue may indicate increased risk of developing the disease

Mutations in the SETD1A gene are rare, but significantly increase patients’ risk of schizophrenia and neurodevelopmental disorders

ANGPTL4 mutations can reduce patients’ risk of heart attack by up to 50 percent – so could neutralizing the gene offer a new route to prevention?

New software can reconstruct T cell receptor sequences from RNA sequencing data

A new study reveals that screening for mutations in patients with advanced lung cancer can focus their treatment options and improve success rates

A blood test for circulating tumor DNA can reveal what’s going on below the surface of malignant melanoma

Molecular testing is changing the face of healthcare. But how far should it go?

The Penn State Hershey Institute for Personalized Medicine benefits from a unique “build it as you need it” growth pattern

Penn Medicine’s Center for Personalized Diagnostics is on a mission to improve patient care using the power of genomics

How is fierce ambition translated into the reality of building two world-class personalized healthcare institutes?