Saphetor caught up with Constantia Aristidou from The Cyprus Institute of Neurology & Genetics (CING), that highlighted the breadth and scope of VarSome Clinical in their recently published paper; Exploring the Genetic Causality of Discordant...

New York and Lausanne, Switzerland - January 10, 2019 - Saphetor SA, the creator of VarSome, announced today a partnership with the Englander Institute for Precision Medicine at Weill Cornell Medicine, the creator of Precision Medicine Knowledgebase...

VarSome thriving community will soon reach 100,000 users, a significant milestone, and we’d like to thank you for your continuous use of the platform.

We have recently published an article titled VarSome: The Human Genomic Variant Search Engine in Bioinformatics journal ofOxford Academic, so if you use VarSome for your workplease cite itin your articles and all other communications.

Lausanne, Switzerland - November 26, 2018 - Saphetor SA, a Swiss precision medicine company and a leader in diagnostic and bioinformatics solutions for clinical Next Generation Sequencing, announced today that Dr. Erik Zmuda has become a member of...

I’d like to welcome you to VarSome’s first quarterly sum up. But before we start, I’d like to take this opportunity to introduce myself as a new member of VarSome’s team serving the position of Head of Business Development. I believe my scientific...

The course NGS in DNA Diagnostics course was held at Medical Faculty of Erasmus University in Rotterdam, The Netherlands, between 4th and 6th of September 2018 and was focused on genomic sequencing in medical diagnostic context, i.e how to apply ...

This is approved reprint article of GenomeWeb’s Saphetor’s VarSome Search is Latest Step on Road to Community of Genomics Professionals, published on June 26, 2018, by Neil Versel.

Since its first launch 3 years ago, VarSome has become a hugely popular platform among clinicians & researchers. We would love to hear from you to understand how you use the platform and how you’d like to see it evolve.