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21 results on '"Morón‐Duran, Francisco D."'

3. Supplementary Table 1 from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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5. supplementary material legends from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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6. Supplementary Table 5 from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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7. Supplementary Table 2 from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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8. Supplementary Table 8 from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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9. Supplementary Table 7 from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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10. Data from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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11. Supplementary Table 3 from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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13. Supplementary Table 4 from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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14. Supplementary Table 6 from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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15. Supplementary Figures from Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, primary, Paré-Brunet, Laia, primary, Lázaro, Kira, primary, Bellido, Fernando, primary, Alonso, M. Henar, primary, Aussó, Susanna, primary, Guinó, Elisabet, primary, Beltrán, Sergi, primary, Castro-Giner, Francesc, primary, Gut, Marta, primary, Sanjuan, Xavier, primary, Closa, Adria, primary, Cordero, David, primary, Morón-Duran, Francisco D., primary, Soriano, Antonio, primary, Salazar, Ramón, primary, Valle, Laura, primary, and Moreno, Victor, primary

Published
2023
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16. ICO Amplicon NGS Data Analysis: A Web Tool for Variant Detection in Common High-Risk Hereditary Cancer Genes Analyzed by Amplicon GS Junior Next-Generation Sequencing

Author

Lopez-Doriga, Adriana, Feliubadaló, Lídia, Menéndez, Mireia, Lopez-Doriga, Sergio, Morón-Duran, Francisco D., del Valle, Jesús, Tornero, Eva, Montes, Eva, Cuesta, Raquel, Campos, Olga, Gómez, Carolina, Pineda, Marta, González, Sara, Moreno, Victor, Capellá, Gabriel, and Lázaro, Conxi

Published
2014
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19. Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer

Author

Sanz-Pamplona, Rebeca, primary, Lopez-Doriga, Adriana, additional, Paré-Brunet, Laia, additional, Lázaro, Kira, additional, Bellido, Fernando, additional, Alonso, M. Henar, additional, Aussó, Susanna, additional, Guinó, Elisabet, additional, Beltrán, Sergi, additional, Castro-Giner, Francesc, additional, Gut, Marta, additional, Sanjuan, Xavier, additional, Closa, Adria, additional, Cordero, David, additional, Morón-Duran, Francisco D., additional, Soriano, Antonio, additional, Salazar, Ramón, additional, Valle, Laura, additional, and Moreno, Victor, additional

Published
2015
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20. ICO amplicon NGS data analysis: a web tool for variant detection in common high-risk hereditary cancer genes analyzed by amplicon GS junior next-Generation Sequencing

Author

Universitat Politècnica de Catalunya. Departament d'Enginyeria Electrònica, Universitat Politècnica de Catalunya. (TIEG) - Terrassa Industrial Electronics Group, López Dóriga, Adriana, Feliubadalo, Lidia, Menendez, Maria Dolores, Lopez Doriga, Sergio, Morón Duran, Francisco D., del Valle, Jesús, Tornero, Eva, Montes, Eva, Cuesta, Raquel, Campos, Olga, Gómez, Carolina, Pineda, Marta, González, Sara, Moreno, Victor, Capellá Frau, Gabriel José, Lázaro, Conxi, Universitat Politècnica de Catalunya. Departament d'Enginyeria Electrònica, Universitat Politècnica de Catalunya. (TIEG) - Terrassa Industrial Electronics Group, López Dóriga, Adriana, Feliubadalo, Lidia, Menendez, Maria Dolores, Lopez Doriga, Sergio, Morón Duran, Francisco D., del Valle, Jesús, Tornero, Eva, Montes, Eva, Cuesta, Raquel, Campos, Olga, Gómez, Carolina, Pineda, Marta, González, Sara, Moreno, Victor, Capellá Frau, Gabriel José, and Lázaro, Conxi

Abstract

Next-generation sequencing (NGS) has revolutionized genomic research and is set to have a major impact on genetic diagnostics thanks to the advent of benchtop sequencers and flexible kits for targeted libraries. Among the main hurdles in NGS are the difficulty of performing bioinformatic analysis of the huge volume of data generated and the high number of false positive calls that could be obtained, depending on the NGS technology and the analysis pipeline. Here, we present the development of a free and user-friendly Web data analysis tool that detects and filters sequence variants, provides coverage information, and allows the user to customize some basic parameters. The tool has been developed to provide accurate genetic analysis of targeted sequencing of common high-risk hereditary cancer genes using amplicon libraries run in a GS Junior System. The Web resource is linked to our own mutation database, to assist in the clinical classification of identified variants. We believe that this tool will greatly facilitate the use of the NGS approach in routine laboratories., Peer Reviewed, Postprint (published version)

Published
2013

21. ICO Amplicon NGS Data Analysis: A Web Tool for Variant Detection in Common High-Risk Hereditary Cancer Genes Analyzed by Amplicon GS Junior Next-Generation Sequencing

Author

Lopez-Doriga, Adriana, primary, Feliubadaló, Lídia, additional, Menéndez, Mireia, additional, Lopez-Doriga, Sergio, additional, Morón-Duran, Francisco D., additional, del Valle, Jesús, additional, Tornero, Eva, additional, Montes, Eva, additional, Cuesta, Raquel, additional, Campos, Olga, additional, Gómez, Carolina, additional, Pineda, Marta, additional, González, Sara, additional, Moreno, Victor, additional, Capellá, Gabriel, additional, and Lázaro, Conxi, additional

Published
2013
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