학술논문

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학술논문
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'학술논문' 에서의 검색결과 28건 | 목록 1~10

  • 7 .
    Pan-cancer analysis of whole genomes
    저자
    by Campbell, P. J. a.; Abpemail, Author; Getz, G. b.; C, D; Eemail, Author, et al. 
    소스
    Nature, vol 578, iss 7793
    Semple, C 2020, ' Pan-cancer analysis of whole genomes ', Nature, vol. 578, no. 7793, pp. 82-93 . https://doi.org/10.1038/s41586-020-1969-6
    Nature, 578, 82-93. Nature Publishing Group
    The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium, Bristow, R, Hayes, S, Wedge, D & et al. 2020, ' Pan-cancer analysis of whole genomes ', Nature. https://doi.org/10.1038/s41586-020-1969-6
    ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium, Weischenfeldt, J L, Sidiropoulos, N, Brunak, S & Rodriguez Gonzalez, F G 2020, ' Pan-cancer analysis of whole genomes ', Nature, vol. 578, no. 7793, pp. 82-93 . https://doi.org/10.1038/s41586-020-1969-6
    Digital.CSIC. Repositorio Institucional del CSIC
    instname
    ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium, Collaborators (2020). Pan-cancer analysis of whole genomes. Nature, 578(7793), pp. 82-93. Springer Nature 10.1038/s41586-020-1969-6
    Nature (London), 578 (7793
    Nature
    Scopus
    RUO. Repositorio Institucional de la Universidad de Oviedo
    Nature, 578(7793), 82-93. Nature Publishing Group
    Nature, 578, 7793, pp. 82-93
    Nature, 578 (7793)
    NATURE
    Dipòsit Digital de Documents de la UAB
    Universitat Autònoma de Barcelona
    The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium 2020, ' Pan-cancer analysis of whole genomes ', Nature, vol. 578, no. 7793, pp. 82-93 . https://doi.org/10.1038/s41586-020-1969-6
    Dipòsit Digital de la UB
    Universidad de Barcelona
    Nature, 578, 82-93
    RUO: Repositorio Institucional de la Universidad de Oviedo
    Universidad de Oviedo (UNIOVI)
    UPCommons. Portal del coneixement obert de la UPC
    Universitat Politècnica de Catalunya (UPC)
  • 7 .
    Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
    저자
    by Bailey, Matthew H; Meyerson, William U; Dursi, Lewis Jonathan; Wang, Liang-Bo; Dong, Guanlan, et al. 
    소스
    Nature Communications, 11(1):4748. Nature Publishing Group
    Nature communications, 11(1):4748. Nature Publishing Group
    Nature communications, 11 (1
    NATURE COMMUNICATIONS
    Nature Communications, 11 (1)
    Nature Communications, Vol 11, Iss 1, Pp 1-27 (2020)
    Bailey, M H, Meyerson, W U, Dursi, L J, Wang, L B, Dong, G, Liang, W W, Weerasinghe, A, Li, S, Kelso, S, Akbani, R, Anur, P, Bailey, M H, Buchanan, A, Chiotti, K, Covington, K, Creason, A, Ding, L, Weischenfeldt, J, Brunak, S, Ding, L, Favero, F, MC3 Working Group, PCAWG novel somatic mutation calling methods working group & PCAWG Consortium 2020, ' Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples ', Nature Communications, vol. 11, no. 1, 4748 . https://doi.org/10.1038/s41467-020-18151-y
    Bailey, Matthew H; Meyerson, William U; Dursi, Lewis Jonathan; Wang, Liang-Bo; Dong, Guanlan; Liang, Wen-Wei; Weerasinghe, Amila; Li, Shantao; Kelso, Sean; Saksena, Gordon; Ellrott, Kyle; Wendl, Michael C; Wheeler, David A; Getz, Gad; Simpson, Jared T; Gerstein, Mark B; Ding, Li (2020). Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples. Nature Communications, 11(1), p. 4748. Springer Nature 10.1038/s41467-020-18151-y
    Nature communications, vol 11, iss 1
    Dipòsit Digital de Documents de la UAB
    Universitat Autònoma de Barcelona
    RUO. Repositorio Institucional de la Universidad de Oviedo
    instname
    Nature Communications
    Dipòsit Digital de la UB
    Universidad de Barcelona
    Nature Communications, 11, 1
    Recercat. Dipósit de la Recerca de Catalunya
    Digital.CSIC. Repositorio Institucional del CSIC
    Nature Communications, 11
    RUO: Repositorio Institucional de la Universidad de Oviedo
    Universidad de Oviedo (UNIOVI)
    Bailey, M H, Meyerson, W U, Dursi, L J, Wang, L B, Dong, G, Liang, W W, Weerasinghe, A, Li, S, Kelso, S, Akbani, R, Anur, P, Bailey, M H, Buchanan, A, Chiotti, K, Covington, K, Creason, A, Ding, L, MC3 Working Group, PCAWG novel somatic mutation calling methods working group & PCAWG Consortium 2020, ' Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples ', Nature Communications, vol. 11, no. 1, 4748 . https://doi.org/10.1038/s41467-020-18151-y
    Recercat: Dipósit de la Recerca de Catalunya
    Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
  • 7 .
    Sex differences in oncogenic mutational processes
    저자
    by Li C. H.; Prokopec S. D.; Sun R. X.; Yousif F.; Schmitz N., et al. 
    소스
    Nature Communications, 11 (1)
    Nature communications, vol 11, iss 1
    11:4330
    Nature Communications
    Li, C H, Prokopec, S D, Sun, R X, Yousif, F, Schmitz, N, PCAWG Tumour Subtypes and Clinical Translation, Boutros, P C & PCAWG Consortium 2020, ' Sex differences in oncogenic mutational processes ', Nature Communications, vol. 11, 4330 . https://doi.org/10.1038/s41467-020-17359-2
    Nature Communications, 11
    Digital.CSIC. Repositorio Institucional del CSIC
    instname
    Li, Constance H; Prokopec, Stephenie D; Sun, Ren X; Yousif, Fouad; Schmitz, Nathaniel; Boutros, Paul C (2020). Sex differences in oncogenic mutational processes. Nature communications, 11(1), p. 4330. 10.1038/s41467-020-17359-2
    RUO. Repositorio Institucional de la Universidad de Oviedo
    Nature communications, 11 (1
    Nature communications, 11(1):4330. Nature Publishing Group
    NATURE COMMUNICATIONS
    Nature Communications, 11, 1
    Li, C H, Prokopec, S D, Sun, R X, Yousif, F, Schmitz, N, Boutros, P C, PCAWG Tumour Subtypes and Clinical Translation & Brunak, S 2020, ' Sex differences in oncogenic mutational processes ', Nature Communications, vol. 11, no. 1, 4330 . https://doi.org/10.1038/s41467-020-17359-2
    Nature Communications, Vol 11, Iss 1, Pp 1-24 (2020)
    Dipòsit Digital de la UB
    Universidad de Barcelona
    Li, C H, Prokopec, S D, Sun, R X, Yousif, F, Schmitz, N & Boutros, P C 2020, ' Sex differences in oncogenic mutational processes ', Nat Commun, vol. 11, no. 1, pp. 4330 . https://doi.org/10.1038/s41467-020-17359-2
    Nature Communications, 11(1):4330. Nature Publishing Group
  • 7 .
    INFRAFRONTIER-providing mutant mouse resources as research tools for the international scientific community
    저자
    by Meehan, TF; Chen, CK; Koscielny, G; Relac, M; Wilkinson, P, et al. 
    소스
    Nucleic Acids Res. 53, D1171-D1175 (2015)
    Nucleic Acids Research
    Repositório Científico de Acesso Aberto de Portugal
    Repositório Científico de Acesso Aberto de Portugal (RCAAP)
    instacron:RCAAP
    Nucleic Acids Research, 43(D1), D1171-D1175. Oxford University Press
    Nucleic acids research (2014). doi:10.1093/nar/gku1193
    info:cnr-pdr/source/autori:INFRAFRONTIER Consortium (Mehaan TF. et al. ... Massimi M., Matteoni R., Tocchini-Valentini GP. ...)/titolo:INFRAFRONTIER-providing mutant mouse resources as research tools for the international scientific community/doi:10.1093%2Fnar%2Fgku1193/rivista:Nucleic acids research/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume
  • 7 .
    Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
    저자
    by Huang, J; Howie, B; Mccarthy, S; Memari, Y; Walter, K, et al. 
    소스
    Nature Communications, 6, 8111
    Nature Communications, 6, pp. 8111
    Nature Communications
    Huang, J, Howie, B, McCarthy, S, Memari, Y, Walter, K, Min, J L, Danecek, P, Malerba, G, Trabetti, E, Zheng, H-F, Gambaro, G, Richards, J B, Durbin, R, Timpson, N J & Marchini, J & Soranzo, N 2015, ' Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel ', Nature Communications, vol. 6, pp. 8111 . https://doi.org/10.1038/ncomms9111
    Huang, J, Howie, B, Mccarthy, S, Memari, Y, Walter, K, Min, J L, Danecek, P, Malerba, G, Trabetti, E, Zheng, H, Al Turki, S, Amuzu, A, Anderson, C A, Anney, R, Antony, D, Artigas, M S, Ayub, M, Bala, S, Barrett, J C, Barroso, I, Beales, P, Benn, M, Bentham, J, Bhattacharya, S, Birney, E, Blackwood, D, Bobrow, M, Bochukova, E, Bolton, P F, Bounds, R, Boustred, C, Breen, G, Calissano, M, Carss, K, Pablo Casas, J, Chambers, J C, Charlton, R, Chatterjee, K, Chen, L, Ciampi, A, Cirak, S, Clapham, P, Clement, G, Coates, G, Cocca, M, Collier, D A, Cosgrove, C, Cox, T, Craddock, N, Crooks, L, Curran, S, Curtis, D, Daly, A, Day, I N M, Day-williams, A, Dedoussis, G, Down, T, Du, Y, Van Duijn, C M, Dunham, I, Edkins, S, Ekong, R, Ellis, P, Evans, D M, Farooqi, I S, Fitzpatrick, D R, Flicek, P, Floyd, J, Foley, A R, Franklin, C S, Futema, M, Gallagher, L, Gasparini, P, Gaunt, T R, Geihs, M, Geschwind, D, Greenwood, C, Griffin, H, Grozeva, D, Guo, X, Guo, X, Gurling, H, Hart, D, Hendricks, A E, Holmans, P, Huang, L, Hubbard, T, Humphries, S E, Hurles, M E, Hysi, P, Iotchkova, V, Isaacs, A, Jackson, D K, Jamshidi, Y, Johnson, J, Joyce, C, Karczewski, K J, Kaye, J, Keane, T, Kemp, J P, Kennedy, K, Kent, A, Keogh, J, Khawaja, F, Kleber, M E, Van Kogelenberg, M, Kolb-kokocinski, A, Kooner, J S, Lachance, G, Langenberg, C, Langford, C, Lawson, D, Lee, I, Van Leeuwen, E M, Lek, M, Li, R, Li, Y, Liang, J, Lin, H, Liu, R, Lönnqvist, J, Lopes, L R, Lopes, M, Luan, J, Macarthur, D G, Mangino, M, Marenne, G, März, W, Maslen, J, Matchan, A, Mathieson, I, Mcguffin, P, Mcintosh, A M, Mckechanie, A G, Mcquillin, A, Metrustry, S, Migone, N, Mitchison, H M, Moayyeri, A, Morris, J, Morris, R, Muddyman, D, Muntoni, F, Nordestgaard, B, Northstone, K, O'donovan, M C, O'rahilly, S, Onoufriadis, A, Oualkacha, K, Owen, M J, Palotie, A, Panoutsopoulou, K, Parker, V, Parr, J R, Paternoster, L, Paunio, T, Payne, F, Payne, S J, Perry, J R B, Pietilainen, O, Plagnol, V, Pollitt, R C, Povey, S, Quail, M A, Quaye, L, Raymond, L, Rehnström, K, Ridout, C K, Ring, S, Ritchie, G R S, Roberts, N, Robinson, R L, Savage, D B, Scambler, P, Schiffels, S, Schmidts, M, Schoenmakers, N, Scott, R H, Scott, R A, Semple, R K, Serra, E, Sharp, S I, Shaw, A, Shihab, H A, Shin, S, Skuse, D, Small, K S, Smee, C, Smith, G D, Southam, L, Spasic-boskovic, O, Spector, T D, St Clair, D, St Pourcain, B, Stalker, J, Stevens, E, Sun, J, Surdulescu, G, Suvisaari, J, Syrris, P, Tachmazidou, I, Taylor, R, Tian, J, Tobin, M D, Toniolo, D, Traglia, M, Tybjærg-Hansen, A, Valdes, A M, Vandersteen, A M, Varbo, A, Vijayarangakannan, P, Visscher, P M, Wain, L V, Walters, J T R, Wang, G, Wang, J, Wang, Y, Ward, K, Wheeler, E, Whincup, P, Whyte, T, Williams, H J, Williamson, K A, Wilson, C, Wilson, S G, Wong, K, Xu, C, Yang, J, Zaza, G, Zeggini, E, Zhang, F, Zhang, P, Zhang, W, Gambaro, G, Richards, J B, Durbin, R, Timpson, N J, Marchini, J & Soranzo, N 2015, ' Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel ', Nature Communications, vol. 6, 8111 . https://doi.org/10.1038/ncomms9111
  • 7 .
    Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
    저자
    by Colonna, V; Ayub, Q; Chen, Y; Pagani, L; Luisi, P, et al. 
    소스
    Genome Biology, 15(6):R88. BMC
    Recercat. Dipósit de la Recerca de Catalunya
    instname
    Genome Biology
    CONICET Digital (CONICET)
    Consejo Nacional de Investigaciones Científicas y Técnicas
    instacron:CONICET
    GenomeBiology.com (Lond., Print) 15 (2014). doi:10.1186/gb-2014-15-6-r88
    info:cnr-pdr/source/autori:Colonna, Vincenza; Ayub, Qasim; Chen, Yuan; Pagani, Luca; Luisi, Pierre; Pybus, Marc; Garrison, Erik; Xue, Yali; Tyler-Smith, Chris/titolo:Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences/doi:10.1186%2Fgb-2014-15-6-r88/rivista:GenomeBiology.com (Lond., Print)/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume:15
    Genome Biology : Biology for the Post-Genomic Era
    Digital.CSIC. Repositorio Institucional del CSIC
    Genome biology
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