Rare Disease Day 2022

Clinical trials are the backbone of modern medicine, responsible for bringing innovative, safe, and efficient treatments to market after rigorous…

Medical advancement relies on clinical trials, which are essential for the development of safe and effective innovative treatments. However, the…

Discover how matched tumor-normal sequencing can help clinical researchers detect the somatic origin of variants with certainty.

We recently presented two posters at the European Congress of Pathology 2024, in Florence, Italy, in collaboration with Janssen Pharmaceutical,…

See how Henry Ford Health enhanced their genetic testing by adopting exome sequencing for hereditary cancer, cystic fibrosis, and pharmacogenetics…

In response to the emerging needs in global healthcare, SOPHiA GENETICS has just revealed the New Generation SOPHiA DDM™ Platform,…

ESMO updated its recommendations for NGS in advanced cancers this year, urging broader use of NGS in additional cancer types…

We recently spoke with Manuela Badiali, Rita Congiu, and Stefania Murru from the Laboratory of Genetics and Genomics, Microcitemico Pediatric…

In this piece, we talked to the two presenters of the poster “The Validation of a Homologous Recombination Deficiency Assay…

Let’s answer some of the most pressing questions about IVDR compliance in practice and explore how CE-IVD certified software solutions…

We recently sat down to talk with Katherine Lafferty, MS, CGC about how Alamut™ Visual Plus helps her overcome the…

Watch our poster spotlight interview, hosting Dr.Gardenia Vargas from Hospital del Mar in Barcelona, Spain discussing the poster presentation at…