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DOI 10.1038/s41588-025-02290-3

Медицинская библиотека · Nature genetics · 2025

The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease.

Yépez Vicente A, Demidov German, Ellwanger Kornelia, Laurie Steven, Luknárová Rebeka, Joseph Maran Midhuna Immaculate, Hentrich Thomas, Sagath Lydia, van der Sanden Bart, Astuti Galuh, Neveling Kornelia, Batlle-Masó Laura, Beijer Danique, Brechtmann Felix, Caballero-Oteyza Andrés, Dabad Marc, Denommé-Pichon Anne-Sophie, Doornbos Cenna, Eddafir Zakaria, Estévez-Arias Berta, Kilicarslan Ozge Aksel, Kolen Ingrid H M, Kraß Leon, Lohmann Katja, Londhe Shubhankar, López-Martín Estrella, Maassen Kars, Macken William, Martínez-Delgado Beatriz, Mei Davide, Mertes Christian, Minardi Raffaella, Morsy Heba, Mueller Juliane S, Natera-de Benito Daniel, Nelson Isabelle, Oud Machteld M, Paramonov Ida, Picó Daniel, Piscia Davide, Polavarapu Kiran, Raineri Emanuele, Savarese Marco, Smal Noor, Steehouwer Marloes, Steyaert Wouter, Swertz Morris A, Thomsen Mirja, Töpf Ana, Van de Vondel Liedewei, van der Vries Gerben, Vitobello Antonio, Wilke Carlo, Zurek Birte, Solve-RD DITF-EPICARE, Solve-RD DITF-ITHACA, Solve-RD DITF-EURO-NMD, Solve-RD DITF-RITA, Solve-RD DITF-RND, Solve-RD consortium, T' Hoen Peter-Bram, Matalonga Leslie, Vissers Lisenka E L M, Gilissen Christian, Schulze-Hentrich Julia, Beltran Sergi, Esteve-Codina Anna, Hoischen Alexander, Gagneur Julien, Graessner Holm

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Аннотация

Despite advances in genomic diagnostics, the majority of individuals with rare diseases remain without a confirmed genetic diagnosis. The rapid emergence of advanced omics technologies, such as long-read genome sequencing, optical genome mapping and multiomic profiling, has improved diagnostic yield but also substantially increased analytical and interpretational complexity. Addressing this complexity requires systematic multidisciplinary collaboration, as recently demonstrated by targeted diagnostic workshops. Here, we highlight the experience of the Solve-RD consortium, a pan-European initiative, in implementing four structured workshops, termed 'Solvathons', as a regular and effective component of its operational workflow. We provide actionable insights, best practices and lessons learned for successful data integration, expert training and scalable collaborative diagnostics within large research consortia.

Для цитирования: Yépez Vicente A, Demidov German, Ellwanger Kornelia, Laurie Steven, Luknárová Rebeka, Joseph Maran Midhuna Immaculate, Hentrich Thomas, Sagath Lydia, van der Sanden Bart, Astuti Galuh, Neveling Kornelia, Batlle-Masó Laura, Beijer Danique, Brechtmann Felix, Caballero-Oteyza Andrés, Dabad Marc, Denommé-Pichon Anne-Sophie, Doornbos Cenna, Eddafir Zakaria, Estévez-Arias Berta, Kilicarslan Ozge Aksel, Kolen Ingrid H M, Kraß Leon, Lohmann Katja, Londhe Shubhankar, López-Martín Estrella, Maassen Kars, Macken William, Martínez-Delgado Beatriz, Mei Davide, Mertes Christian, Minardi Raffaella, Morsy Heba, Mueller Juliane S, Natera-de Benito Daniel, Nelson Isabelle, Oud Machteld M, Paramonov Ida, Picó Daniel, Piscia Davide, Polavarapu Kiran, Raineri Emanuele, Savarese Marco, Smal Noor, Steehouwer Marloes, Steyaert Wouter, Swertz Morris A, Thomsen Mirja, Töpf Ana, Van de Vondel Liedewei, van der Vries Gerben, Vitobello Antonio, Wilke Carlo, Zurek Birte, Solve-RD DITF-EPICARE, Solve-RD DITF-ITHACA, Solve-RD DITF-EURO-NMD, Solve-RD DITF-RITA, Solve-RD DITF-RND, Solve-RD consortium, T' Hoen Peter-Bram, Matalonga Leslie, Vissers Lisenka E L M, Gilissen Christian, Schulze-Hentrich Julia, Beltran Sergi, Esteve-Codina Anna, Hoischen Alexander, Gagneur Julien, Graessner Holm. The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease.. Nature genetics. 2025. DOI: 10.1038/s41588-025-02290-3.

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