Výsledky vyhledávání - "Picó Amador, Daniel"

Akademický článek

Remote visualization of large-scale genomic alignments for collaborative clinical research and diagnosis of rare diseases

Publikováno v: In Cell Genomics 8 February 2023 3(2)

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The RD-connect genome-phenome analysis platform: accelerating diagnosis, research, and gene discovery for rare diseases

Autor: Laurie, Steven, Piscia, Davide, Matalonga, Leslie, Corvó, Alberto, Fernández-Callejo, Marcos, Garcia-Linares, Carles, Hernandez-Ferrer, Carles, Luengo, Cristina, Martínez, Inés, Papakonstantinou, Anastasios, Picó-Amador, Daniel, Protasio, Joan, Thompson, Rachel, Tonda, Raul, Bayés, Mònica, Bullich, Gemma, Camps-Puchadas, Jordi, Paramonov, Ida, Trotta, Jean-Rémi, Alonso, Angel, Attimonelli, Marcella, Béroud, Christophe, Bros-Facer, Virginie, Buske, Orion J, Cañada-Pallarés, Andrés, Fernández, José M, Hansson, Mats G, Horvath, Rita, Jacobsen, Julius O B, Kaliyaperumal, Rajaram, Lair-Préterre, Séverine, Licata, Luana, Lopes, Pedro, López-Martín, Estrella, Mascalzoni, Deborah, Monaco, Lucia, Pérez-Jurado, Luis A, Posada De la Paz, Manuel, Rambla, Jordi, Rath, Ana, Riess, Olaf, Robinson, Peter N, Salgado, David, Smedley, Damian, Spalding, Dylan, 't Hoen, Peter A C, Töpf, Ana, Zaharieva, Irina, Graessner, Holm, Gut, Ivo G, Lochmüller, Hanns, Beltran, Sergi, Corvo, Alberto, Garcia, Carles, Fernandez‐Callejo, Marcos, Hernandez, Carles, Ntalis, Anastasios Papakonstantinou, Protassio, Joan, Martinez, Ines, Pico, Daniel, Bayes, Monica, Camps, Jordi, Trotta, Jean‐Remi, Bros‐Facer, Virginie, Buske, Orion, Cañada, Andrés, Fernandez, Josè Maria, Hansson, Mats, Jacobsen, Julius, Lair, Severine, López‐Martin, Estrella, Jurado, Luis Pérez, Posada, Manuel, Robinson, Peter, Spalding, Dylan J., 't Hoen, Peter‐Bram, Gut, Ivo, Lochmúller, Hanns

Publikováno v: Human Mutation: Variation, Informatics and Disease, 43(6), 717-733. WILEY
Academica-e. Repositorio Institucional de la Universidad Pública de Navarra
instname
Human Mutation

Rare disease patients are more likely to receive a rapid molecular diagnosis nowadays thanks to the wide adoption of next-generation sequencing. However, many cases remain undiagnosed even after exome or genome analysis, because the methods used miss

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ff0fc29121e729a92e245623f303623
https://hdl.handle.net/2454/43348

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Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases

Autor: 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

Publikováno v: 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

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 co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0d359958be1dbfc846fb31cb9015358
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85129716393&doi=10.1016/j.jmoldx.2022.02.003&partnerID=40&md5=c9b38d123b890e9a622b4f0023e8f719

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Sistemes de monitoratge

Autor: Picó Amador, Daniel

Publikováno v: O2, repositorio institucional de la UOC
Universitat Oberta de Catalunya (UOC)

Els sistemes de monitoratge són essencials avui dia a complexes xarxes de computadors. Aquests ens garanteixen que totes les errades produïdes a la xarxa són detectades i informen els operadors per tal de solucionar-les. Aquest treball està div

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6e3a26ca78dc14d4517a8fd9744b30a6

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