Apply any of these PhD/ postdoc funding calls to work with rare disease multiomics, pangenome, episignatures, repetitive elements:

📣The official programme for the 14th CNAG Symposium is live! 9⃣ Leading experts will share cutting-edge insights in #CancerGenomics, don’t miss it! 🗓️ Dec 16 | 09:00–16:15 📍 Auditori Antoni Caparrós, @PCB_UB (Barcelona) 👉 https://t.co/hGkHASLjVK #CNAGSymposium #CNAG

🌍Yesterday, our PhD student @tmontsay from the Functional Genomics Team presented his poster at #EMBOMobileGenome on 'A Comprehensive Annotation of Conserved Protein Domains in Human Endogenous Retroviruses' 🙌Excellent work and insightful discussions! @AEsteveCodina

🚨Webinar alert! Today, our Functional Genomics Team Leader, @AEsteveCodina, will discuss the value of RNA-seq and long-read genome and methylome data in rare disease diagnosis 🗓️11:00 CEST https://t.co/MlgUpajh67 By @NGSCN_de & @UniklinikAachen #Genomics #RareDiseases #CNAG

💜 Even better news from the #Unicas_Hackathon! 5⃣ families have finally received a diagnosis after 48 hours of intense collaboration among international experts A huge step forward for #RareDiseases and, most importantly, for these children Proud to be part of this initiative!

🙌¡Maratón por las enfermedades raras! 💜Ayer empezaba el primer Únicas Hackathon, un encuentro de clínicos, investigadores y genetistas para hallar el diagnóstico de 12 casos pediátricos en 48 horas 🧬Como colaboradores, nuestro equipo fue hasta Murcia para ayudar a la causa

📢New paper out in @NatureGenet! ✨CNAG coordinates the Solvathons, a groundbreaking pan-European initiative for rare disease diagnosis @Solve_RD launched these interdisciplinary workshops, which have led to 100 new diagnoses for rare disease families 📎 https://t.co/RMs4DEjaC4

🙌New advances on rare diseases! Within the @Solve_RD, @PacBio HiFi long-read whole-genome sequencing has proven instrumental in uncovering previously undetectable genetic variants, leading to new diagnoses https://t.co/lVScqq1MOg #RareDiseases #CNAG @genomeresearch @ERDERA_org

🚨New job offer! ➡️Join the Functional Genomics Team at CNAG as a Bioinformatician to work on the SEED-ALS Spain project, a national initiative focused on understanding and treating Amyotrophic Lateral Sclerosis (ALS) 🗓️ Apply by 30 September 🔗 https://t.co/bATayQMwG6 #CNAG

📢We’re hiring! Join our team at CNAG and help advance genomics research! Check out our new positions: ➡️Bioinformatician (Functional Genomics Team) ➡️PhD Student - Computational Biologist (Single Cell Team) 🔗 https://t.co/bATayQN4vE #Jobs #Hiring #Genomics #ResearchJobs

🌍 Today is World RNA Day! Discover with our Functional Genomics Team Leader, @AEsteveCodina, why RNA is a vital biological key: essential for advancing research in cancer, rare diseases 🌟At CNAG, we study RNA to improve people's health and quality of life #RNADay #RNA #CNAG

📢New paper in Neuromuscular disorders (@WorldMuscleSoc)! 🧬A study helped identify a new genetic variant in the TNNT3 gene causing a rare muscle disorder in two siblings, thanks to a multi-omics approach (genomics and transcriptomics) 📎 https://t.co/Dvc07rbndM #RareDiseases

4/ Low MALAT1 levels (e.g., <1% of median) are reliable indicators of damaged cells or low-quality nuclei in snRNA-seq. read 10x Q&A

7/ In Tabula Muris and Tabula Sapiens, MALAT1 expression was tightly correlated with nuclear RNA content and intronic fractions.

Best Poster in Clinical Research Rebeka Luknárová, Munich, Germany P16.006.A - "Harmonized framework for RNA-seq-based rare disease diagnostics in a pan-continental consortium - Solve-RD"

🙌 Really excited about this recognition! Congratulations to our partners from @TU_Muenchen — Rebeka Luknárová, @vaym88, and Julien Gagneur — together with our Functional Genomics Team Leader at CNAG, @AEsteveCodina, and @Solve_RD #research #eshg2025 #bestposter

🔥Non-stop on the last day of #eshg2025! 🗣️This morning we joined the oral presentation of our partner @vaym88 (@TU_Muenchen): 'Rare Disease Solvathons – the power of multi-omics data integration'. Truly inspiring work! #RareDiseases #CNAG #GenomicsIsInOurDNA #Research

🧬Great presentation by our Functional Genomics Team Leader, @AEsteveCodina, at #eshg2025! 🗣️She showcased our work on “Integrative multi-omics for undiagnosed Rare Diseases (Omics-RD)” 👏 Congratulations, Anna, and well done to the team behind this project! #RareDiseases #CNAG

🔝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

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