QIAGEN Digital Insights

DYK: yearly, more than 134M patients experience adverse drug events, causing 2.4M deaths worldwide 💀 What if safer, more effective drugs could be developed based on a person’s unique DNA? On Nov. 13, meet our game-changing tool that will let labs and pharma companies effectively use complex #pharmacogenomics (PGx) data for #drugdevelopment. Learn more 👉 https://lnkd.in/gPTqTEHR

We are excited to announce that COSMIC v101 will be released this month! Keep an eye on our socials throughout November for sneak peeks into this next update 🎉 🧬 #CancerResearch #Genomics

Ignite your curiosity. Challenge the norm. Push the boundaries of knowledge. QIAGEN Biomedical Knowledge Base does more than simple databases – it connects the dots, helping you unlock the secrets hidden within your data. ▶️ Ready to embrace your inner Einstein? 👉 https://lnkd.in/gZ47DhVn

From Diwali to Thanksgiving, November’s proving to be a precious month to mark triumphs and other things to be grateful for. 🙏🙇 While we fill the air with festive cheer, let us also stock up on "brain gear" 😉 Don’t miss out on our November events ➡️ https://lnkd.in/g7yvC8y7

It’s almost November, yet we’re still buzzing from the memories of our first-ever Data Science Day in Europe 🤩 A huge thank you to all our participants, presenters and organizers for your time and energy! Can’t wait for the next one 👌

✈️ We’ll be at the American Society of Human Genetics Annual Meeting in Denver, CO! Drop by booth 618 to explore our Sample to Insight solutions, and don’t miss our featured talk by Dr. David Bick on the Newborn Genomes Programme at Genomics England, where they use QCI Interpret at testing sites throughout the UK for #variantinterpretation and reporting for #WGS data of 100,000 newborns 👶 Learn more 👉 https://lnkd.in/gvxJw3qx #genomics #ASHG2024 #humangenetics

Big news – and it’s a game-changer for pharmacogenomics! 💊 Introducing QIAGEN Pharmacogenomic Insights (PGXI), a new expert-curated knowledgebase for labs and pharma companies to rapidly decode how genetic variations affect drug response. This one tool offers: ☑️ Centralized access to multiple PGx sources ☑️ Automated PGx annotation – in minutes! ☑️ Flexible and scalable integration into workflows Check it out 👉 https://lnkd.in/gpYmrUPf

Newsflash: Expert curation outperforms AI in precision by 126%?! 🤯 Check out this 2024 independent, peer-reviewed study from The National Institutes of Health that puts #HGMD Professional head-to-head with 3 literature mining tools for variant curation. The results speak for themselves 👉 https://lnkd.in/gsfepdS5

Few spots left! 🏃 Applications for our #QCIInterpret for #Oncology workshop are only open for 2 more days. Register now and get the chance to experience this industry-leading clinical decision support software firsthand 👉 https://lnkd.in/gA3CfHJa

✅ Working in pharma and ✅ eyeing the AI-Driven #DrugDiscovery Summit on your calendar? Kick off the summit with our in-person #KnowledgeGraph workshop! You have everything to gain: 👨💼 Hear from and engage with industry experts 💻 Exclusive access to live demos and case studies, including #competitiveintelligence 💰 FREE pass to the rest of the summit Apply now ➡️ https://lnkd.in/gDrZUTi9