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Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.

E. Rheinbay, M. Nielsen, F. Abascal, J. Wala, O. Shapira, G. Tiao, H. Hornshøj, J. Hess, R. Juul, Z. Lin, L. Feuerbach, R. Sabarinathan, T. Madsen, J. Kim, L. Mularoni, S. Shuai, A. Lanzós, C. Herrmann, Y. Maruvka, C. Shen, S. Amin, P. Bandopadhayay, J. Bertl, K. Boroevich, J. Busanovich, J. Carlevaro-Fita, D. Chakravarty, C. Chan, D. Craft, P. Dhingra, K. Diamanti, N. Fonseca, A. Gonzalez-Perez, Q. Guo, M. Hamilton, N. Haradhvala, C. Hong, K. Isaev, T. Johnson, M. Juul, A. Kahles, A. Kahraman, Y. Kim, J. Komorowski, K. Kumar, S. Kumar, D. Lee, K. Lehmann, Y. Li, E. Liu, L. Lochovsky, K. Park, O. Pich, N. Roberts, G. Saksena, S. Schumacher, N. Sidiropoulos, L. Sieverling, N. Sinnott-Armstrong, C. Stewart, D. Tamborero, J. Tubio, H. Umer, L. Uusküla-Reimand, C. Wadelius, L. Wadi, X. Yao, C. Zhang, J. Zhang, J. Haber, A. Hobolth, M. Imielinski, M. Kellis, M. Lawrence, C. von Mering, H. Nakagawa, B. Raphael, M. Rubin, C. Sander, L. Stein, J. Stuart, T. Tsunoda, D. Wheeler, R. Johnson, J. Reimand, M. Gerstein, E. Khurana, P. Campbell, N. López-Bigas, G. Bader, J. Barenboim, R. Beroukhim, S. Brunak, K. Chen, J. Choi, J. Deu-Pons, J. Fink, J. Frigola, C. Passerini, D. Garsed, G. Getz, I. Gut, D. Haan, A. Harmanci, M. Helmy, E. Hodzic, J. Izarzugaza, J. Kim, J. Korbel, E. Larsson, S. Li, X. Li, S. Lou, K. Marchal, I. Martincorena, A. Martínez-Fundichely, P. McGillivray, W. Meyerson, F. Muiños, M. Paczkowska, K. Park, J. Pedersen, T. Pons, S. Pulido-Tamayo, I. Reyes-Salazar, M. Reyna, C. Rubio-Perez, S. Sahinalp, L. Salichos, M. Shackleton, R. Shrestha, A. Valencia, M. Vazquez, L. Verbeke, J. Wang, J. Warrell, S. Waszak, J. Weischenfeldt, G. Wu, J. Yu, X. Zhang, Y. Zhang, Z. Zhao, L. Zou, K. Akdemir, E. Alvarez, A. Baez-Ortega, P. Boutros, D. Bowtell, B. Brors, K. Burns, K. Chan, I. Cortés-Ciriano, A. Dueso-Barroso, A. Dunford, P. Edwards, X. Estivill, D. Etemadmoghadam, M. Frenkel-Morgenstern, D. Gordenin, B. Hutter, D. Jones, Y. Ju, M. Kazanov, L. Klimczak, Y. Koh, E. Lee, J. Lee, A. Lynch, G. MacIntyre, F. Markowetz, M. Meyerson, S. Miyano, F. Navarro, S. Ossowski, P. Park, J. Pearson, M. Puiggròs, K. Rippe, S. Roberts, B. Rodriguez-Martin, R. Scully, D. Torrents, I. Villasante, N. Waddell, J. Wala, L. Yang, S. Yoon, and J. Zamora. Nat., 578 (7793): 102-111 (2020)

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Specific small-RNA signatures in the amygdala at premotor and motor stages of Parkinson's disease revealed by deep sequencing analysis.L. Pantano, M. Friedländer, G. Escaramís, E. Lizano, J. Pallarès-Albanell, I. Ferrer, X. Estivill, and E. Martí. Bioinformatics, 32 (5): 673-681 (2016)Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation.H. Susak, L. Serra-Saurina, G. Demidov, R. Rabionet, L. Domènech, M. Bosio, F. Muyas, X. Estivill, G. Escaramís, and S. Ossowski. PLoS Comput. Biol., (2021)Probe-specific mixed-model approach to detect copy number differences using multiplex ligation-dependent probe amplification (MLPA).J. González, J. Carrasco, L. Armengol, S. Villatoro, L. Jover, Y. Yasui, and X. Estivill. BMC Bioinformatics, (2008)Genome sequencing data analysis for rare disease gene discovery.U. Umlai, D. Bangarusamy, X. Estivill, and P. Jithesh. Briefings Bioinform., (2022)Accounting for uncertainty when assessing association between copy number and disease: a latent class model.J. González, I. Subirana, G. Escaramís, S. Peraza, A. Cáceres, X. Estivill, and L. Armengol. BMC Bioinformatics, (2009)SNPassoc: an R package to perform whole genome association studies.J. González, L. Armengol, X. Solé, E. Guinó, J. Mercader, X. Estivill, and V. Moreno. Bioinformatics, 23 (5): 654-655 (2007)Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.E. Rheinbay, M. Nielsen, F. Abascal, J. Wala, O. Shapira, G. Tiao, H. Hornshøj, J. Hess, R. Juul, Z. Lin and 179 other author(s). Nat., 578 (7793): 102-111 (2020)A non-biased framework for the annotation and classification of the non-miRNA small RNA transcriptome.L. Pantano, X. Estivill, and E. Martí. Bioinformatics, 27 (22): 3202-3203 (2011)

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Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.

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copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.

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Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.