Saphetor SA receives IVDR Certification for clinical diagnosis support NGS data analysis platform, VarSome Clinical, ensuring enhanced safety and performance standards https://t.co/m1F1KLjYTw
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! https://t.co/WZuYb3iqwj
We’re #hiring! Do you have a background in #bioinformatics or #productmanagement? Do you want to apply your talents and passion to making a very real difference in people’s lives? Let's talk! https://t.co/RwI9gfSj4w
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 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: https://t.co/hgJDcoITwK
#Genomics#VariantInterpretation#Bioinformatics#IVDR
"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 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!
Visiting Toronto for #ACMGMtg24 but sad that the Maple Leafs aren't in town? Drop by our booth to pick up a stress-relieving Saphetor hockey puck to get your hockey fix as you learn about @varsome 🏒 🍁
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!
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!
Are you ready for this?! 🎉#FOG2024
Mark your calendars, the UK's largest #genomics event is back on home turf & returning to London on 24th & 25th January 2024 at ExCeL!
Register for your ticket: https://t.co/gt3lCj8rKr
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.
This map shows the connections our users have made around specific variants. With over 3 000 papers citing @varsome , we must be doing something right!
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:
https://t.co/et5fAanaG0
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 https://t.co/dw8eKcZVFV is free to use wherever you live 🌎🌍🌏
With over 140 data sources and a community spread over 124 countries, we’re helping to make sure that everyone has access to comprehensive human #genome variant information. Improving human health for everyone is a global effort!
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: https://t.co/et5fAamCQs
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!
We're looking for people who are passionate about improving human #health by exploring what's possible with human #genome data. If that sounds like you, then we'd love to hear from you! Here's a list of our open positions: https://t.co/pCd5KoiJad
#hiringnow
Visualize publication trends with our publications timeline viewer, displaying data on PubMed articles relating to your gene or variant of interest.
Try it today: https://t.co/QNE1S6YQ7I
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: https://t.co/wGcC5dbZnK