
Universitat Pompeu Fabra
Articles
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Jan 16, 2025 |
bmcpublichealth.biomedcentral.com | José Augusto |Josep Maria |van Staalduinen |Universitat Pompeu Fabra
Fifty-six individuals (mean age 40 years (range 24–83), 62% women) registered in the two-day multidisciplinary Aging towards walkable futures workshop held in Barcelona (Table 1). A summary of the discussions held during this event is presented below, following the structure of its four thematic Sessions.
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Jan 7, 2025 |
journals.plos.org | Universitat Pompeu Fabra |Clàudia Salat-Canela |Guillem Murciano-Julià |Marina Francos-Cárdenas
Loading metrics Open Access Peer-reviewed Methods and Resources Methods and Resources report novel methods, substantial improvements to current methodologies, or informational datasets. See Journal Information» Citation: Murciano-Julià G, Francos-Cárdenas M, Salat-Canela C, Hidalgo E, Ayté J (2025) FLCCR is a fluorescent reporter system that quantifies the duration of different cell cycle phases at the single-cell level in fission yeast. PLoS Biol 23(1): e3002969.
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Jan 5, 2025 |
journals.plos.org | Universitat Pompeu Fabra
Loading metrics Open Access Peer-reviewedResearch Article ? This is an uncorrected proof. Citation: Páscoa dos Santos F, Verschure PFMJ (2025) Excitatory-inhibitory homeostasis and bifurcation control in the Wilson-Cowan model of cortical dynamics. PLoS Comput Biol 21(1): e1012723.
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Dec 9, 2024 |
journals.plos.org | Xavier Escriba-Montagut |Universitat Pompeu Fabra |Yannick Marcon |Augusto Anguita-Ruiz
Citation: Escriba-Montagut X, Marcon Y, Anguita-Ruiz A, Avraam D, Urquiza J, Morgan AS, et al. (2024) Federated privacy-protected meta- and mega-omics data analysis in multi-center studies with a fully open-source analytic platform. PLoS Comput Biol 20(12): e1012626. https://doi.org/10.1371/journal.pcbi.1012626Editor: Gamze Gursoy, Yale University, UNITED STATES OF AMERICAReceived: October 27, 2023; Accepted: November 10, 2024; Published: December 9, 2024Copyright: © 2024 Escriba-Montagut et al.
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Dec 2, 2024 |
academic.oup.com | Universitat Pompeu Fabra
Advances in high-throughput DNA sequencing technologies and decreasing costs have fueled the identification of small genetic variants (such as single nucleotide variants and indels) across tumors. Despite efforts to standardize variant formats and vocabularies, many sources of variability persist across databases and computational tools that annotate variants, hindering their integration within cancer genomic analyses.
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