- A positive response to therapy in a paediatric patient with a renal rhabdoid tumour has enabled researchers to identify immune cells with anti tumour activity in this rare cancer, which affects roughly of 12 children per year in Spain and has an extremely low survival rate. - After receiving...

- A new open-source toolkit turns complex phenotypic data into actionable insights, accelerating the discovery of rare disease diagnoses and aids cohort building for cross-disease analytics. - Pheno-Ranker helps researchers classify patients and find similar cases with just a few clicks, by...

- The project is part of an international collaboration supported by The Mark Foundation’s ASPIRE grant, co-funded by the...

- Researchers from the Centro Nacional de Análisis Genómico (CNAG, Spain), together with the St. Jude Children’s Research Hospital (USA) and the University of Adelaide (Australia), have developed a revolutionary...

At CNAG, as coordinators of the IMPaCT-Genómica sequencing network, we present this outreach video showcasing the collaborative work behind Spain’s national genome sequencing infrastructure. The network brings together three leading centres—CNAG in Barcelona...

- A new review, recently published in Biomolecules, analyzes the current opportunities and challenges of mass spectrometry-based proteomics in the investigation of genetic muscle diseases. - The review —a joint effort between the CNAG, the Leibniz Institute for Analytical Sciences (ISAS), and the...