🙌 Proud of our talent! Our Master’s student Monique Saclolo presented her master’s project: “Systematic Assessment of Genetic Newborn Screening Approaches”, supervised by our Clinical Genomics Manager @lmatalonga.bsky.social & Data Analyst Claire Morgan Congrats, Monique! @geneticsub.bsky.social

🙌Yesterday we had the pleasure of welcoming the participants of the @eurordis.bsky.social #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 #CNAG

🎯At #ESHG2025, ERDERA showcased its bold vision to transform rare disease diagnostics across Europe—scaling Solve-RD’s success to 100,000+ cases with cutting-edge tech and cross-border collaboration. 🔗 Read more: loom.ly/qv98Csg ‪ #ERDERA

⏱️Want to get to know CNAG in just 1 minute? 🧬Discover what we achieve last year and our international team, collaborations, sequencing capacity & applications, computing power, and our top research! For more info, visit: www.cnag.eu #eshg2025 #milan #GenomicsIsInOurDNA #CNAG #eshg @eshgsociety

🔝Day 3 at #eshg2025 — see what we’re up to! ➡️10:30 – Increased diagnosis rate in rare diseases through iterative re-analysis and multi-omics integration ➡️11:00 – Integrative multi-omics for undiagnosed rare diseases ➡️13:00 – Does genome analysis quality matter? #CNAG #eshg #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. Well done, Gemma! #Genomics #RareDiseases #MultiOmics #GenomicsIsInOurDNA

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

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

🇮🇹Still going strong in Milan at #eshg2025! 🗣️Our Clinical Genomics Manager ‪@lmatalonga.bsky.social presented the latest advances from Screen4Care — accelerating rare disease diagnosis through two key pillars: genetic newborn screening and digital technologies #RareDiseases #Horizon2020 #CNAG

🎉Exciting moments at #eshg2025! We welcomed our partner Ximo García from @pacbio.bsky.social to the CNAG booth (382) 🧬We’re proud to have Revio, one of the latest sequencing platforms from the company, up and running in our facilities #CNAG #LongReadSequencing #GenomicsIsInOurDNA

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

⏳4 days left until #eshg2025! 📌Come and say hi to CNAG at stand 382 🧬We're here to help make your science a reality — contributing to prevention, diagnosis and treatment across a wide range of diseases 🗣️Our presentations and posters: ccnag-my.sharepoint.com/:b:/g/person... @eshg.bsky.social‬

🔝Gaceta Médica publica un súper artículo sobre CNAG! 📰"El Centro Nacional de Análisis Genómico ha cerrado 2024 con un balance que consolida su papel como uno de los pilares científicos de la medicina de precisión en España y Europa" Red. Jefe: @delsanz.bsky.social gacetamedica.com/investigacio...

🇮🇹Milan, here we go! CNAG will be at #ESHG2025 — find us at booth 382! Pass by and discover how we’re advancing human genomics, hereditary cancer, and rare diseases 🗣️Want to arrange a meeting with us? Drop us a line at [email protected]. See you there! Organised by @eshg.bsky.social

📺 Sortim al Telenotícies de TV3! Sabíeu que el CNAG contribuirà a crear el primer catàleg d'ADN de la població europea? 🧬 Seqüenciarem 6.000 genomes de la població espanyola 🎯 L'objectiu és obtenir el genoma de referència de les diferents poblacions europees per impulsar la medicina de precisió

🔬Saps quins són els hubs i initiatives científiques a Catalunya en l'àmbit de les ciències de la vida i la salut? Aquí teniu el mapa amb les 50 infraestructures que impulsem la innovació per la salut de les persones. 🌍Som referents a Europa! ➡️@biocat.cat: www.biocat.cat/ca/sala-de-p...

🚀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! 📎https://goo.su/CVNR #CNAG #AnnualReport #ICTS

🙌¡Hoy hemos recibido la visita de nuestro Consejo Rector! 👥Nos han acompañado los representantes del Ministerio de Ciencia, Innovación y Universidades y de la Generalitat de Catalunya 🧬Una jornada muy completa, en la que han conocido la Sala de Secuenciación y el Centro de Procesamiento de Datos

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

💜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

🚀 EASIGEN takes off – Europe’s largest genomics research infrastructure! 🌍 Proud to coordinate this initiative, uniting 13 top infrastructures across Europe with the capacity to sequence 500K genomes per year 🔗 www.cnag.eu/news/easigen... #EASIGEN @easigen-eu.bsky.social #CNAG #HorizonEU #Genomics

💜 Rare, but not alone! 🌍 On #RareDiseaseDay, we stand with the families who have been waiting years for a diagnosis At CNAG, it’s our mission to help improve their quality of life by identifying the genetic causes 📹Press play! #RareDiseases #MoreThanYouCanImagine #Research #CNAG #TogetherForRare

🙌 El CNAG surt a @elsmatins.bsky.social de TV3! ➡️ Descobreix un dels últims estudis on hem ajudat a més de 500 famílies amb malalties minoritàries a trobar el seu diagnòstic. Un projecte europeu, coliderat pel CNAG www.linkedin.com/feed/update/... #DiaMalaltiesRares #RareDiseaseDay #ElsMatinsTV3

🌟Great News: CNAG is now on BlueSky! 🚀From Barcelona to the world, we’re bringing you the latest in genomics! Stay tuned for breaking news, cutting-edge technologies, groundbreaking research, and upcoming events 🔗https://www.cnag.eu #Genomics #Innovation #Research #BlueSky #CNAG