Héritas to distribute VarSome Clinical in Argentina

Posted by Tomas Kucera on Jul 3, 2019 12:03:10 PM

Lausanne, Switzerland – July 3, 2019 - Saphetor SA, a Swiss precision-medicine company and leader in diagnostic and bioinformatics solutions for clinical Next Generation Sequencing (NGS), announced today a distribution agreement with Héritas SA, an Argentinian precision-medicine company. Saphetor’s VarSome Clinical, a clinically-certified platform for interpretation of NGS data extends Héritas’s portfolio of tools and services for a wide range of its clients employing NGS technologies for clinical as well as for research purposes.

VarSome as Human Genomics Community

Posted by Tomas Kucera on Feb 14, 2019 10:56:04 AM
 
As a researcher or medical professional, you may encounter a rare variant which you have never seen before. Collecting information about such a variant may take you a lot of time without any guarantee that you will find what you need. However, if there was another clinician or researcher, anywhere in the world, who has already dealt with the same variant in the past and if there was an easy way to get in touch, well, everything would be much easier. And that's what VarSome as a  Human Genomics Community is all about!

PMKB now available on VarSome!

Posted by Tomas Kucera on Jan 10, 2019 2:22:41 PM

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 (PMKB), a curated resource for the clinical interpretation of cancer variants [1]. PMKB is now a fundamental component of VarSome’s portfolio of over 30 integrated and cross-referenced public data resources as well as VarSome’s implementation of the American College of Medical Genetics guidelines.

VarSome 6.7 has been released

Posted by Richard Meyer on Dec 13, 2018 2:49:50 PM

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.

Cite VarSome!

Posted by Andreas Massouras on Nov 29, 2018 12:59:04 PM

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.

Dr. Erik Zmuda becomes a member of VarSome's Advisory Board

Posted by Tomas Kucera on Nov 26, 2018 11:04:29 AM

Banner - LI 1 - Nov

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 its Advisory Board.