Bernardo Rodriguez Martin
@BerniRdgz
Independent Fellow at @CRG. Leading the Repetitive DNA Biology (REPBIO) Team
*New Open-Access Long Read Resource*. We sequenced 1,019 genomes from the 1000 Genomes Project sample cohort using @nanopore. Sequencing data is available at bit.ly/4m8dlE2. @embl @HHU_de @IMPvienna @CRGenomica nature.com/articles/s4158… [1/8]
Call for papers! 📣
Call for Papers! @genomeresearch is now encouraging submissions for a Special Issue on The Genetics and Genomics of Somatic Mosaicism, Guest Edited by Drs. @giladevrony, @EAliceLee2, and @R_Rahbari. tinyurl.com/Call-for-paper… #BOG25 #KSMosaicism25 #MITS25 #somaticmosaicism
(1/3) The @EU_Commission has proposed to double the funding for Horizon Europe to €175B in the next long-term budget (2028-2034): europa.eu/!F68v7J This signals the programme’s role as a key pillar of Europe’s innovation – because good solutions start with solid science.
Very promising news on the next seven-year EU budget, with a proposed substantial increase for Horizon Europe including the ERC. We are analysing the other parts of this proposal in more detail. @Vonderleyen @EZaharievaEU research-and-innovation.ec.europa.eu/news/all-resea…
#PacBio is contributing Iso-Seq data to the 1000 Genomes Long Read Sequencing Project using #Kinnex kits and the #Revio system. This data from 1,000 globally diverse samples will help advance transcript-level insights across populations. Press release: bit.ly/4mdzHEe
La resecuenciación de 1.019 genomas 🧬que publica @Nature "constituye la referencia más completa de evaluación genética estructural del genoma humano". ➡Lo cuenta @BerniRdgz, del @CRGenomica ✍@pilar_pj diariomedico.com/medicina/genet…
EMBL researchers and their collaborators have provided exciting new insights into human genetic variation by building upon the 1000 Genomes Project dataset. The two studies constitute what may be the most complete overview of the human genome to date. embl.org/news/science/b…
Hi folks! come find me on Bluesky: @bernardo-rodriguez.bsky.social 😉
A more complete understanding of human genetics starts with accurate, high-quality reference genomes. HPRC is building a reference that reflects the breadth of human genetic variation, supporting better prediction, diagnosis, and treatment. Learn more: humanpangenome.org/samples/
📅 En septiembre vuelven nuestras ayudas a talento: prácticas, predoctorales, postdocs… Consulta ya el calendario provisional 2025/2026 de convocatorias AECC 👉 contraelcancer.es/sites/default/… El calendario podría actualizarse. Síguenos para no perderte nada. #AyudasAECC…
🔍We are looking for 1–2 early-career Group Leaders to join our thriving international research community. 📌 Why choose @NCMBMnews ? 🤝Group leader Biswa Sahu: "There’s a real spirit of cooperation here; people are generous with their time, their expertise, and their ideas."
An emerging polishing pipeline, DeepPolisher, improves genome assemblies by reducing indel errors and correcting false homozygosity. Applied to 180+ HPRC assemblies, it cut errors by 54% and significantly boosted overall quality. Here’s how… genome.cshlp.org/content/35/7/1…