💭 Do you interpret and analyse genetic variants? We’re looking for participants to take part in our short survey to help us better understand the stakeholders that could use our variant interpretation solution. Take part now and enter our prize draw: eu1.hubs.ly/H08MQ340

Excited to be attending the Genomics England Research Summit today! Looking forward to learning from industry experts and exploring the latest advancements in genomics research. See you there! #GERS2024 #RareDisease #Genomics

🎉 We’re thrilled to announce that in our next product release, we will be introducing our secondary analysis service integrated with AION. Simplify your workflow! Curious to learn more? Check your eligibility and get early access to the platform: eu1.hubs.ly/H0cs_t-0

🎉 We’re thrilled to announce that we have launched Secondary Analysis (FASTQ to VCF) integrated with AION. Streamline your variant analysis workflow and elevate your variant interpretation capabilities. Curious to learn more? Click here to get access eu1.hubs.ly/H0cN2bQ0

Traditional genetic variant interpretation is complex and time-consuming, posing challenges for small labs. AI-driven tools like AION simplify workflows, enabling faster, more accurate diagnoses. Learn more in our latest article eu1.hubs.ly/H0cYXbr0

🔎 Is your lab's variant interpretation taking too long and costing too much? Accelerate your workflow with our AI-driven variant prioritisation — the fastest way to pinpoint relevant variants in just 5-10 minutes, starting at €35 per case! Get in touch! eu1.hubs.ly/H0d2kcv0

Mark your calendars & join us for a Live demo & Q&A, with our team of experts Aina Pi Roig & Pablo Botas, showcasing & introducing you to AION. 📅 Date: Wednesday 6th November, 2024 🕒 Time: 11:00 am CET / 10:00 am GMT 👉 Secure your spot now: eu1.hubs.ly/H0d96Jb0

🔎 The goal of genomic labs is to find answers. Our latest blog shows how Nostos' new secondary analysis feature creates an efficient workflow—from raw sequencing to clinical insights—allowing labs to get results faster. Read more here: eu1.hubs.ly/H0dcfTR0

👀 Don't forget - Join us for a Live demo & Q&A, with our team of experts Aina Pi Roig & Pablo Botas, showcasing & introducing you to AION. 📅 Date: Wednesday 6th November, 2024 🕒 Time: 11:00 am CET / 10:00 am GMT 👉 Secure your spot now: eu1.hubs.ly/H0dmTXC0

WES vs. WGS: interpreting genomic variants in complex regions like homopolymers is challenging. Discrepancies highlight the need for careful validation. AI tools like AION (CE-IVD) are reshaping cost-effectiveness and accuracy. Read more here: eu1.hubs.ly/H0dp6p-0

👀 Don't forget - Join us for a Live demo & Q&A tomorrow, with our team of experts Aina Pi Roig & Pablo Botas, showcasing & introducing you to AION. 📅 Date: Wednesday 6th November, 2024 🕒 Time: 11:00 am CET / 10:00 am GMT 👉 Secure your spot now: eu1.hubs.ly/H0dtf3Y0

Stand Out in the Genetic Testing Market – Join Our Webinar! Get insights from the Co-founder of Dilemma Solutions and HealthInCode on building reputation through quality, innovation, and specialized knowledge. Date: 19th Nov, 11:00 (CET) Register now 👉 eu1.hubs.ly/H0dyWXY0

Calling All Rare Disease Researchers! We’re thrilled to launch the AION Research Grant Program for academics working on rare disease diagnostics! ✅ 20 Free Sample Runs (€1,000 value) ✅ Double your sample runs beyond the free ones. Apply here: eu1.hubs.ly/H0dFlLr0 🧑‍🔬🧬

Don’t miss our webinar on Nov 19th! Join industry leader Lorenzo Monserrat - Co-Founder of Dilemma Solutions & Cardiology expert as he shares his expertise on how labs can stand out with quality, specialization, and innovation. Register now 👉 eu1.hubs.ly/H0dGRCg0

At the recent Undiagnosed Disease Hackathon event, our technology made a profound impact, as Professor Alexander Hoischen from Radboud University Medical Center shared. Are you a Rare Disease Researcher? Apply now for the AION Research Grant Program: eu1.hubs.ly/H0dLK5h0

👀 Our Webinar has been moved to 26th November, so there is still time to register for the event! Join Our Co-founder Rocío Acuña Hidalgo and Lorenzo Monserrat - an industry leader with a remarkable track record in cardiology and genetic diagnostics: eu1.hubs.ly/H0dNWqg0

The AION Research Grant Program is your opportunity to revolutionize rare disease diagnostics using cutting-edge AI technology. ✅ 20 Free Sample Runs (€1,000 value) ✅ Double your sample runs beyond the free ones. Only 10 spots available, so act fast: eu1.hubs.ly/H0dPXS80

👀 Less than a week to go! Join our Webinar next week and hear from an industry leader with a remarkable track record in cardiology and genetic diagnostics. If you’re seeking to elevate your lab’s unique value, register now: eu1.hubs.ly/H0dSlLx0

🚨 Last Chance to Register! 🚨 Join us tomorrow for a webinar that explores how genetic testing labs can stand out through quality, specialization, and innovation.💡Don’t miss your chance to gain practical insights for lab differentiation! Register here: eu1.hubs.ly/H0dWgVf0

💡 In Case You Missed It! The AION Research Grant Program is OPEN! 🚀 📢 What’s in it for you? ✔️ 20 Free Sample Runs ✔️ Double additional sample runs purchased ✔️ Access CE-IVD certified AI excellence 🔗 Apply now & elevate your rare disease research: eu1.hubs.ly/H0dWhx_0