Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases
| العنوان: | Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases |
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| المؤلفون: | Bullich, Gemma, Matalonga, Leslie, Pujadas, Montserrat, Papakonstantinou, Anastasios, Piscia, Davide, Tonda, Raúl, Artuch, Rafael, Gallano, Pia, Garrabou, Glòria, González, Juan R., Grinberg, Daniel, Guitart, Míriam, Laurie, Steven, Lázaro, Conxi, Luengo, Cristina, Martí, Ramon, Milà, Montserrat, Ovelleiro, David, Parra, Genís, Pujol, Aurora, Tizzano, Eduardo, Macaya Ruiz, Alfons, Palau, Francesc, Ribes, Antònia, Pérez-Jurado, Luis A., Beltran, Sergi, Schlüter, Agatha, Rodriguez-Palmero, Agustí, Cáceres, Alejandro, Nascimento, Andrés, García-Cazorla, Àngels, Cueto-González, Anna, Marcé-Grau, Anna, Ruiz Nel Lo, Anna, Martínez-Monseny, Antonio, Sànchez, Aurora, García, Belén, Pérez-Dueñas, Belén, Gel, Bernat, Fusté, Berta, Hernández-Ferrer, Carles, Casasnovas, Carlos, Ortez, Carlos, Arjona, César, Hernando-Davalillo, Cristina, Natera de Benito, Daniel, Picó Amador, Daniel, Gómez-Andrés, David, Yubero, Délia, Pelegrí-Sisó, Dolors, Verdura, Edgard, García-Arumí, Elena, Castellanos, Elisabeth, Gabau, Elisabeth, Tobías, Ester, López-Grondona, Fermina, Cardellach, Francesc, Garcia-Garcia, Francesc Josep, Munell, Francina, Tort, Frederic, Aznar, Gemma, Olivé-Cirera, Gemma, Tell, Gemma, Muñoz-Pujol, Gerard, Paramonov, Ida, Blanco, Ignacio, Madrigal, Irene, Valenzuela, Irene, Gut, Ivo, Cusco, Ivon, Trotta, Jean-Rémi, Cruz, Jordi, Diaz-Manera, Jordi, Milisenda, José César, Ma Grau, Josep, Garcia-Villoria, Judit, Armstrong, Judith, Cantó, Judith, Sala-Coromina, Júlia, Rodríguez-Revenga, Laia, Alias, Laura, Gort, Laura, González-Quereda, Lídia, Costa, Mar, Fernández-Callejo, Marcos, López-Sánchez, Marcos, Álvarez-Mora, Maria Isabel, Gut, Marta, Serrano, Mercedes, Raspall-Chaure, Miquel, Del Toro, Mireia, Bayés, Mònica, Baena Díez, Neus, Spataro, Nino, Capdevila, Núria, Ugarteburu, Olatz, Muñoz-Cabello, Patricia, Romero Duque, Penélope, Rabionet, Raquel, Rojas-García, Ricardo, Calvo, Rosa, Urreizti, Roser, Bernal, Sara, Boronat, Susana, Balcells, Susanna, Vendrell, Teresa, Universitat Autònoma de Barcelona |
| المصدر: | JOURNAL OF MOLECULAR DIAGNOSTICS r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau instname The Journal of Molecular Diagnostics |
| بيانات النشر: | ELSEVIER SCIENCE INC, 2022. |
| سنة النشر: | 2022 |
| مصطلحات موضوعية: | biology, rare disease, Computational Biology, Nervous system Diseases, Genomics, Whole Exome Sequencing, Pathology and Forensic Medicine, Malalties del sistema nerviós, Genòmica, Rare Diseases, Exome Sequencing, genomics, Molecular Medicine, Humans, genetics, Exome, human, Malalties rares |
| الوصف: | Many patients experiencing a rare disease remain undiagnosed even after genomic testing. Reanalysis of existing genomic data has shown to increase diagnostic yield, although there are few systematic and comprehensive reanalysis efforts that enable collaborative interpretation and future reinterpretation. The Undiagnosed Rare Disease Program of Catalonia project collated previously inconclusive good quality genomic data (panels, exomes, and genomes) and standardized phenotypic profiles from 323 families (543 individuals) with a neurologic rare disease. The data were reanalyzed systematically to identify relatedness, runs of homozygosity, consanguinity, single-nucleotide variants, insertions and deletions, and copy number variants. Data were shared and collaboratively interpreted within the consortium through a customized Genome-Phenome Analysis Platform, which also enables future data reinterpretation. Reanalysis of existing genomic data provided a diagnosis for 20.7% of the patients, including 1.8% diagnosed after the generation of additional genomic data to identify a second pathogenic heterozygous variant. Diagnostic rate was significantly higher for family-based exome/genome reanalysis compared with singleton panels. Most new diagnoses were attributable to recent gene-disease associations (50.8%), additional or improved bioinformatic analysis (19.7%), and standardized phenotyping data integrated within the Undiagnosed Rare Disease Program of Catalonia Genome-Phenome Analysis Platform functionalities (18%). Supported by Generalitat de Catalunya through Departament de Salut (SLT002/16/00174 to URD-Cat consortium) and Departament d’Empresa i Coneixement and the CERCA Program; FP7 and H2020 EU projects RD-Connect, Solve-RD, and EJP-RD grants FP7 305444, H2020 779257, and H2020 825575 for CNAG-CRG; Spanish Ministry of Science and Innovation to the EMBL partnership and through the Instituto de Salud Carlos III grants PT13/0001/0044 and PT17/0009/0019 for CNAG-CRG and grants PI16/01048, PI19/01310, PI18/00451, PI18/00498, and PI21/00935 for IDIBAPS (Instituto Nacional de Bioinformática); ELIXIR Implementation Studies (CNAG-CRG); Centro de Investigaciones Biomédicas en Red de Enfermedades Raras; Centro de Excelencia Severo Ochoa grant SEV-2016-0571 (CNAG-CRG) and grant CEX 2018-000806-S (ISGLOBAL); and cofinancing with funds from the European Regional Development Fund by the Spanish Ministry of Science and Innovation corresponding to the Programa Operativo FEDER Plurirregional de España (POPE) 2014 to 2020 and by the Secretaria d’Universitats i Recerca, Departament d’Empresa i Coneixement of the Generalitat de Catalunya corresponding to the Programa Operatiu FEDER de Catalunya 2014 to 2020. |
| وصف الملف: | application/pdf |
| تدمد: | 1525-1578 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0d359958be1dbfc846fb31cb9015358Test https://www.scopus.com/inward/record.uri?eid=2-s2.0-85129716393&doi=10.1016/j.jmoldx.2022.02.003&partnerID=40&md5=c9b38d123b890e9a622b4f0023e8f719Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....a0d359958be1dbfc846fb31cb9015358 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 15251578 |
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