VarSome Clinical uses #AI to prioritize suspected causative variants in your #NGS sample. By entering your phenotypic data, VarSome Picks can run its advanced filtering to present you with the most likely variants of interest. Try it out today: landing.varsome.com/varsome-clinic…

Visualize publication trends with our publications timeline viewer, displaying data on PubMed articles relating to your gene or variant of interest. Try it today: varsome.com

Did you know - that some people love VarSome so much, that they've joined our team to work with us full-time? If you've been thinking about working with us, we'd love to hear from you!

Our latest feature, VarSome Picks, is a filter developed with #AI, to prioritize variants with the highest possibility of being causative or associated with the suspected disease or phenotype that the user provides. Try it for yourself today: ​​bit.ly/VarSomeContact

The Saphetor mission: To enable anyone to find, share and use the most comprehensive human genome data – and to collaborate to improve health and lives around the world. That's why VarSome.com is free to use wherever you live 🌎🌍🌏

If you need convincing that VarSome is the perfect #NGS solution for you, here’s what one of our customers has to say. Book a consultation today and find out how VarSome can help you: bit.ly/VarSomeContact

Our users are spread across 6 continents - not only are they able to access one of the most powerful human #genome #variant databases in existence for free, but they are able to connect with each other to help share helpful information that can help save lives all over the world.

We are very excited to share news of our partnership with Oxford Nanopore . We'll be sharing what we've already been working on together at #ASHG2023

We're looking forward to seeing everyone in London next year!

After a great 1st day of exhibiting at #ASHG2023 we only have a handful of VarSome stress balls left! Drop by booth 933 for your chance to win a bluetooth speaker and learn about everything that's new with VarSome, including our work with long reads!

Interested in seeing how we support Oxford Nanopore data? Drop by booth 933 at 12.30pm today at #ASHG

Drop by our booth if you're at #ACMGMtg24 today for a VarSome masterclass. We'll be covering tips and tricks and taking a deep dive with VarSome Clinical!

Drop by our #ACMGMtg24 booth 1408 to get some swag today and tomorrow!

We are down to the final 3 hours here at #ACMGMtg24 - You've still got time to drop by booth 1408 for a guided tour of VarSome and a Saphetor hockey puck!

"What do you like most about VarSome?" Our implementation of ACMG guidelines for our #germline classifier is one of the most popular answers! No blackbox here - you can see exactly which rules have been triggered, and why, as well as the impact on the predicted #pathogenicity

We are expanding our network of distributors so we can support our customers wherever they are. If you're looking for an #NGS analysis solution that will provide you local support, let us know: share.hsforms.com/12fOnjRIsRha4d… #Genomics #VariantInterpretation #Bioinformatics #IVDR

Did you know that VarSome Clinical includes updated #PanelApp gene lists for you to filter by? PanelApp includes all of the gene panels related to genomic tests listed in the NHS Genomic Test Directory and the virtual gene panels used in the 100,000 Genomes Project.

We're hiring!

Saphetor SA receives IVDR Certification for clinical diagnosis support NGS data analysis platform, VarSome Clinical, ensuring enhanced safety and performance standards dlvr.it/TB0CTF

VarSome Clinical is now CE-IVDR certified. A major milestone not only for Saphetor, but the #ClinicalGenomics field. We are among the first #bioinformatics platforms to achieve this! bit.ly/CE-IVDR