🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

📺¡Salimos en Antena 3 Noticias! 🌟Felices de ver en prime time una de nuestras últimas investigaciones en #CNAG, en la que hemos contribuido a encontrar el diagnóstico a más de 500 familias con #EnfermedadesRaras (Dr. @SteveLaurie42 y Dr. Sergi Beltran) 🔗cnag.eu/news/over-500-…

🌟¡Ayer nos entrevistaron en RTVE Noticias! 📺El Dr. Sergi Beltran entró en directo con la gran periodista Ana Belén Roy para explicar los resultados del estudio que ayudó a diagnosticar a más de 500 familias con #EnfermedadesRaras ▶️Vídeo completo: youtu.be/wEkuo_nQNso

🎗️Today is #WorldCancerDay! Did you know that genomics plays a key role in cancer prevention, diagnosis, and treatment? At CNAG, we are committed to advanced cancer research —every step brings us closer to a cure! #CancerResearch #Genomics #Cancer #DiaMundialContraElCancer

💜Today, we celebrate that talent, dedication, and commitment know no gender. At CNAG, equity and inclusion are in our DNA, creating an environment where everyone’s potential is recognised and valued #WomensDay #DiversityMatters #8M #8M2025 #Diadelamujer #DiadelaDona #CNAG

🚀New advances in Screen4Care! At CNAG, we’ve begun processing the first samples, which have already been sequenced 🎯The EU project aims to accelerate rare disease diagnosis through genetic screening and advanced analysis in newborns #RareDiseases #Genomics #Bioinformatics

🚨 Only 3 days left to register! 🚨 Join leading rare disease experts in Warsaw on 10–11 April to shape Europe’s future strategy💡 “Towards an EU Action Plan on Rare Diseases” – 2 days of key discussions & networking 🔗 Register now: loom.ly/ekq3FDg ⏳ Deadline: 3 April!

🚀Excited to share our 2024 Annual Report! 🔝A summary of the key milestones we hit last year, from expanding sequencing capacity to strengthening our role in clinical genomics. 🙌Thanks to all our partners, especially our teams, for making it possible! 📎goo.su/CVNR

🟢 #ENTREVISTA Vicente Yépez: “El análisis de ARN no sustituye al de ADN, pero ayuda en muchos casos a complementarlo” Léelo todo 👉 genotipia.com/genetica_medic… #diagnosticogenetico #geneticamedica #geneticaclinica #genetica #genomica #secuenciacionARN #ARN #variantegenetica #ADN

AJHG latest article presents work from the Solve-RD Consortium that shows how integrated mtDNA analyses improve rare disease diagnostics, even when mitochondrial disorders are not suspected: cell.com/ajhg/fulltext/… #ASHG

🚨Job alert! 🔎We're looking for a Front-End Software Engineer Join us and contribute to key projects in cancer, rare diseases, and immunology, such as Instand-NGS4P or 3TR-IMI 🗓️Deadline: 31 May 📥Applications: cnag.eu/jobs/front-end… #JobAlert #FrontendEngineer #SoftwareJobs

👉Let’s get started at #ESHG2025! 🇪🇺Our team from CNAG is joining the Diagnostic Research Workstream Meeting 2025 as part of ERDERA 🧬We're proud to contribute to the collective effort to improve diagnosis for people living with rare diseases. #RareDiseases #ERDERA #CNAG

👀Ready to dive into the latest study by our Clinical Genomics Manager, Leslie Matalonga? ➡️13-14h. Genetic newborn screening by TREAT panel targeted sequencing in a large European cohort: pipeline design and first output results from the Screen4Care EU project #eshg2025

💪 What a dream team we’ve got at CNAG for #eshg2025 — our super project managers, the Human Genetics and the Functional Genomics Team! 😎And just look how good we look in our new t-shirts… CNAG is giving it all, once again! 📍Find us at booth 382 #GenomicsIsInOurDNA #eshg

👥This is us! The CNAG team at #eshg2025: our Project Managers Elena Vila and Francesc Bou, Clinical Genomics Manager Leslie Matalonga, Functional Genomics Leader AnnaEsteveCodina, Data Analysts Steve Laurie and Gemma Bullich, and our Director Ivo Gut 🗓️Book a meeting with us!

📸 Another moment we’re keeping from #eshg2025: Yesterday we had the pleasure of meeting many of our ERDERA Diagnostic Research Workstream partners in Milan 🧩We're proud to be part of this committed consortium working to advance rare disease diagnostics #RareDiseases

🌇 Wrapping up a great day at #eshg2025 with Edgard Verdura from Hospital Clínic , Eduard Porta from Josep Carreras Leukaemia Research Institute (IJC), and our Clinical Genomics Manager, Leslie Matalonga 🧬Always a pleasure to connect with inspiring professionals in the field #CNAG #GenomicsIsInOurDNA

📍Don’t miss us at the Sequencing Square, Hall 4! 🗓️Monday, 26 May at 11:00 🧬Our Functional Genomics Team Leader at CNAG, AnnaEsteveCodina, is presenting the poster “Integrative multi-omics for undiagnosed Rare Diseases (Omics-RD)” #eshg2025 #RareDiseases #GenomicsIsInOurDNA

🗣️Impressive talk by our Data Analyst Gemma Bullich at #eshg2025! 🧬“Increased diagnosis rate in rare diseases through iterative re-analysis and multi-omics data integration” (C24.01) 👏 So proud of our Human Genetics team #Genomics #RareDiseases #MultiOmics #GenomicsIsInOurDNA

🙌Yesterday we had the pleasure of welcoming the participants of the EURORDIS-Rare Diseases Europe #OpenAcademy2025 🧬They explored our main projects, our Sequencing Unit and Data Center — where science and technology come together to advance rare disease research See you next year! #RareDiseases

🙌 Proud of our talent! Our Master’s student Monique Saclolo has presented her master’s project: “Systematic Assessment of Genetic Newborn Screening Approaches”, supervised by our Clinical Genomics Manager, Leslie Matalonga, & Data Analyst Claire Morgan Congratulations, Monique!