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 of its Advisory Board.
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 authorized distributor of Agilent Technologies for the Czech Republic. Saphetor’s clinically-certified platform for fast and accurate variant discovery, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels extends HPST portfolio of tools and services for a wide range of its clients employing NGS technologies for clinical as well as for research purposes.
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 background, combined with my past experience from the world of Software as a Service technologies and multichannel marketing, provide a solid ground for my future contributions to the project. VarSome is a unique community project in the field of human genetics and genomics and I feel honored to be a part of it.