The Centre for Genomic Medicine aims to use genomics and epigenomics to understand the mechanisms underpinning degenerative disease to advance patient care.

The Federated European Genome-phenome Archive (FEGA) is transforming how sensitive human genomic data is shared and accessed.

A simple genomics blood test could improve treatment and care for childhood epilepsy, but more investment is needed to make access fair and securely join up the data, finds a new study.

Creation of a comprehensive genetic representation for more than 2.5 billion people across the Middle East and South Asia ...

A recent review published in the journal Engineering delves into the significant advancements and potential of CRISPR ...

By analyzing the DNA of Fulani people, researchers led by @HopkinsMedicine revealed a shared genetic component among all ...

Creation of a comprehensive genetic representation for more than 2.5 billion people across the Middle East and South Asia could make a major contribution towards advancing precision medicine.

University of Florida researchers are addressing a critical gap in medical genetic research—ensuring it better represents and ...

Ireland's new directory is designed to ensure that patients receive the most appropriate genetic tests to personalise treatment and improve early disease detection.