🧬 Today is #UndiagnosedDay - a day to raise awareness for the millions living with undiagnosed conditions. We work to empower clinicians in delivering accurate diagnoses. Access the worldwide virtual event : undiagnosed-day.org #UndiagnosedDay2024 #enGenome

🏆 VarChat's paper is among the top 5 most read articles in Bioinformatics! Read more about the first GenAI-based tool designed to find and summarize relevant scientific literature on genomic variants. Access here: lnkd.in/gHyDidjq #VarChat #enGenome #bioinformatics

📣 Calling all ISV 2024 attendees in Porto, Portugal! Make sure to catch our CTO Ivan Limongelli as he takes the stage for a panel discussion on "Enhancing genomic variant interpretation with machine learning models." isv.variome.org/program.html #ISV2024 #AIingenomics #enGenome

🎁 iPhone giveaway and Twist Bioscience's guest talk at our ESHG Corporate Satellite on Saturday, June 1st at 10am! Those attending in person will participate in our iPhone giveaway! Save your seat: lnkd.in/deZdPmpg #ESHG24 #enGenome #genomics #AIinhealthcare

🎉 Our ESHG Corporate Satellite session is just around the corner! Be there for insights on our groundbreaking AI-powered solutions and the chance to win an iPhone for those attending in presence! Save your seat now: lnkd.in/deZdPmpg #ESHG24 #enGenome #genomics

🙌 A huge thanks to everyone who visited our booth, watched our corporate satellite and stopped by our posters at #ESHG2024 We're looking forward to many more insightful discussions and collaborations. See you next year in Milan! 🎉 #ESHG2024 #enGenome #eVai #VarChat #genomics

🎉 Our success case got featured at Amazon Web Services (AWS)! At the Di Venere Hospital in Italy, eVai successfully provided a diagnostic confirmation for an adult male with suspected retinitis pigmentosa after previous genetic tests failed to do so aws.amazon.com/it/blogs/publi…

🔍💡VarChat is designed to simplify your report drafting process by using advanced AI to extract and summarize key variant information from scientific literature. Access now: varchat.engenome.com #Genomics #ClinicalReports #AI #VarChat

eVai seamlessly connects with Amazon S3, BaseSpace, and Element Catalyst to streamline your workflow 🧬 You save time, minimize manual errors, and focus on delivering accurate results faster to your patients. Start your free trial: lnkd.in/dVkZMSM5 #ngsanalysis #eVai

🍫 Last weekend, our team had a great experience at a chocolate factory lab in Torino - a city famous for its chocolates! We got to know about the fascinating world of chocolate creation and get our hands-on, making our very own chocolate bars! #TeamBuilding #enGenome

Our client, Dr. Laura Fontana from ASST Santi Paolo e Carlo, is presenting today at the Training Course on Germline & Somatic Pharmacogenetics! She’ll showcase eVai’s variant calling, CNV detection, & how it streamlines PGx workflows. 🧬 biomedia.net/10248/ #PGx #eVai

SIGU 2024 is in full swing! ⛳ Our workshop yesterday was a great success and we also presented 5 posters discussing our latest advancements. The engagement has been fantastic, and it's clear that innovation is at the forefront of everyone’s minds! 🧬 #SIGU2024 #enGenome

🎃 No tricks, only treats today! Pack your bags and meet us at #ASHG24! We’ll be at booth #333 ready to chat with you! 🧙‍♀️ And as a bonus we are brewing up some big news about VarChat! No magic potions here—just science you can trust! 💪 #enGenome #VarChat #eVai

VarChat mentioned in NCBI's 25-Year celebration article of dbSNP! 🎉 A big congratulations on 25 years of dbSNP and thank you for acknowledging VarChat! 🔗 Read the full article here: lnkd.in/d8KA6F4E #VarChat #dbSNP #NCBI #enGenome

VarChat featured on GenomeWeb! 🚀 VarChat, the first GenAI platform for variant literature mining and summarization, was highlighted in GenomeWeb’s latest article 🔗 Read the full article here: genomeweb.com/informatics/en… #Genomics #VarChat #enGenome #GenerativeAI

New website article! In our latest website article, we discuss: 🔹Why variant interpretation can be a bottleneck and how to fix it 🔹How AI and automation are speeding up diagnosis Read it here: lnkd.in/d5h6NXwj #enGenome #AIinhealthcare #NGS #RareDisease

📢 VarChat is now in @MobiDetails! MobiDetails is an annotation platform developed by MoBiDiC_BioInfo and VarChat is now integrated into their newest address, giving users access to the latest publications on genomic variants and genes. Read more: engenome.com/news/Varchat-o…

We’re heading to GfH 2025 next week in Innsbruck, Austria and we’d love to connect! We are eager to help you cut manual workload, prioritize variants faster and access the literature you need—right when you need it! See you there! #GfH2025 #Genomics #NGS #PrecisionMedicine

Kicked off #GfH2025 with our workshop on real-world challenges in variant interpretation Tools like #eVai and #VarChat were built to help you work faster and smarter. 🎯 Stop by Booth 39 to connect! #Genomics #AIinHealthcare #VariantInterpretation #ClinicalGenetics

Hear from global experts and get a chance to win a free entrance to ESHG 2026! If you want to learn how AI is being used across the globe to make variant assessment more efficient, this is the session to put on your calendar! 👉 Secure your spot now: lnkd.in/dcwct5kH