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 of Oxford Academic, so if you use VarSome for your work please cite it in 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...

Lausanne, Switzerland - November 20, 2018 - Saphetor SA, a Swiss precision-medicine company and leader in diagnostic and bioinformatics solutions for clinical Next Generation Sequencing (NGS), announced today a partnership with HPST, s.r.o., an...

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...

[October 18, 2018 San Diego, USA] Today, at ASHG in San Diego, we are thrilled to announce VarSome PRO, an extended version of VarSome, our popular and widely used genomics search engine.

Over the weekend we released an updated version of VarSome, with a number of improvements across the board, as well as two new databases.

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.

We are announcing the first version of VarSome extension for Chrome browser. It finds variants on a page and links them automatically to VarSome.

Advance Notice. We are changing the Free API Package for existing users. In order to test and evaluate the VarSome API, anyone interested will be given free access to variants in chromosome 17 only (which contains popular genes BRCA1 and TP53),...

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.