Examinant per Autoria "Trotta, Jean-Remi"
Resultats per pàgina
Opcions d'ordenació
Ítem Accés Obert Benchmarking of whole exome sequencing and ad hoc designed panels for genetic testing of hereditary cancer(Nature Research, 2017) Feliubadaló, Lídia; Tonda, Raúl; Trotta, Jean-Remi; Gut, Marta; Gut, Ivo Glynne; Beltran, Sergi; Lázaro García, Conxi
Ítem Accés Obert Framework for quality assessment of whole genome cancer sequences(Nature Research, 2020) Whalley, Justin P.; Stobbe, Miranda D.; Beltran, Sergi; Gut, Marta; Trotta, Jean-Remi; Gut, Ivo Glynne
Ítem Accés Obert From Wet-Lab to Variations: Concordance and Speed of Bioinformatics Pipelines for Whole Genome and Whole Exome Sequencing(Wiley, 2016) Laurie, Steven, 1973-; Fernández Callejo, Marcos; Marco Sola, Santiago; Trotta, Jean-Remi; Camps-Puchadas, Jordi; Chacón, Alejandro; Espinosa, Antonio; Gut, Marta; Gut, Ivo Glynne; Heath, Simon; Beltran, Sergi
Ítem Accés Obert Genotyping-by-sequencing resolves relationships in Polygonaceae tribe Eriogoneae(Wiley, 2021) Pearman, Peter B.; Alioto, Tyler; Trotta, Jean-Remi; Columbus, J. Travis
Ítem Accés Obert Pan-cancer analysis of whole genomes(Nature Research, 2020) ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium; Demidov, German, 1990-; Drechsel, Oliver; Ossowski, Stephan; Estivill, Xavier, 1955-; Escaramís, Geòrgia; Bosio, Mattia; Holik, Aliaksei Z.; Sušak, Hana, 1985-; Rabionet, Raquel; Stobbe, Miranda D.; Marquès i Bonet, Tomàs, 1975-; Navarro i Cuartiellas, Arcadi, 1969-; Gut, Ivo Glynne; Beltran, Sergi; Gut, Marta; Trotta, Jean-Remi; Whalley, Justin P.; Heath, Simon; Prasad, Aparna; Heredia Genestar, José María, 1985-; Sabarinathan, Radhakrishnan; Pich, Oriol; Gonzalez-Perez, Abel; Rubio Pérez, Carlota, 1990-; Tamborero Noguera, David; Mularoni, Loris; Deu-Pons, Jordi; Muiños, Ferran; Muyas Remolar, Francesc, 1992-
Ítem Accés Obert The genetic landscape of inherited retinal diseases in a Mexican cohort: genes, mutations and phenotypes(MDPI, 2021) Villanueva-Mendoza, Cristina; Tusón, Miquel; Apam-Garduño, David; de Castro-Miró, Marta; Tonda, Raúl; Trotta, Jean-Remi; Marfany, Gemma; Valero, Rebeca; Cortés-González, Vianney; Gonzàlez-Duarte, Roser
Ítem Accés Obert The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases(Wiley, 2022) Laurie, Steven, 1973-; Piscia, Davide; Matalonga, Leslie; Corvò, Alberto; Fernández Callejo, Marcos; Garcia-Linares, Carles; Hernandez-Ferrer, Carles, 1987-; Luengo, Cristina; Martínez, Inés; Papakonstantinou Ntalis, Anastasios; Picó-Amador, Daniel; Protasio, Joan; Tonda, Raúl; Bayés, Mònica; Bullich, Gemma; Camps-Puchadas, Jordi; Paramonov, Ida; Trotta, Jean-Remi; Pérez Jurado, Luis Alberto; Rambla de Argila, Jordi; Gut, Ivo Glynne; Lochmüller, Hanns; Beltran, Sergi
Ítem Accés Obert The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome(Nature Publishing Group, 2017) Vidal, Silvia; Brandi, Núria; Pacheco, Paola; Gerotina, Edgar; Blasco, Laura; Trotta, Jean-Remi; Derdak, Sophia; del Mar O'Callaghan, María; García Cazorla, Àngels; Pineda, Mercè; Armstrong, Judith; Rett Working Group