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Promoter capture Hi-C-based identification of recurrent noncoding mutations in colorectal cancer.
Orlando, Giulia; Law, Philip J; Cornish, Alex J; Dobbins, Sara E; Chubb, Daniel; Broderick, Peter; Litchfield, Kevin; Hariri, Fadi; Pastinen, Tomi; Osborne, Cameron S; Taipale, Jussi; Houlston, Richard S.
Afiliación
  • Orlando G; Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
  • Law PJ; Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
  • Cornish AJ; Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
  • Dobbins SE; Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
  • Chubb D; Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
  • Broderick P; Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
  • Litchfield K; Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
  • Hariri F; McGill University and Genome Quebec Innovation Centre, Department of Human Genetics, McGill University, Montreal, Quebec, Canada.
  • Pastinen T; McGill University and Genome Quebec Innovation Centre, Department of Human Genetics, McGill University, Montreal, Quebec, Canada.
  • Osborne CS; Center for Pediatric Genomic Medicine, Children's Mercy, Kansas City, MO, USA.
  • Taipale J; Department of Medical and Molecular Genetics, King's College London, London, UK.
  • Houlston RS; Division of Functional Genomics and Systems Biology, Department of Medical Biochemistry and Biophysics, and Department of Biosciences and Nutrition, Karolinska Institutet, Stockholm, Sweden.
Nat Genet ; 50(10): 1375-1380, 2018 10.
Article en En | MEDLINE | ID: mdl-30224643
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Transformación Celular Neoplásica / Cromosomas Humanos / Codón sin Sentido / Biología Computacional / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Diagnostic_studies Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Transformación Celular Neoplásica / Cromosomas Humanos / Codón sin Sentido / Biología Computacional / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Diagnostic_studies Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article