VarSome retweetledi
Saphetor SA receives IVDR Certification for clinical diagnosis support NGS data analysis platform, VarSome Clinical, ensuring enhanced safety and performance standards dlvr.it/TB0CTF
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VarSome
2.3K posts
VarSome
@varsome
The Human Genomic Variant Search Engine
Lausanne, Switzerland Katılım Mayıs 2016
273 Takip Edilen773 Takipçiler
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
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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
GIF
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"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
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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!
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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!
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We're looking forward to seeing everyone in London next year!
Front Line Genomics@FLGenomics
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: hubs.la/Q026fV1q0
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VarSome retweetledi
We are very excited to share news of our partnership with @nanopore . We'll be sharing what we've already been working on together at #ASHG2023
Oxford Nanopore@nanopore
Today, we announce a partnership with @saphetor to provide integrated end-to-end solutions — from sample to report — for comprehensive analysis of nanopore sequencing data to improve the interpretation of rare & undiagnosed diseases. Read more: bit.ly/3tUPbXu
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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.
Saphetor@saphetor
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!
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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
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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 🌎🌍🌏
Saphetor@saphetor
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!
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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
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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!
Saphetor@saphetor
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: bit.ly/saphetorjobs #hiringnow
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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
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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…
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