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Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.
Zhou, Jian; Park, Christopher Y; Theesfeld, Chandra L; Wong, Aaron K; Yuan, Yuan; Scheckel, Claudia; Fak, John J; Funk, Julien; Yao, Kevin; Tajima, Yoko; Packer, Alan; Darnell, Robert B; Troyanskaya, Olga G.
Afiliación
  • Zhou J; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.
  • Park CY; Graduate Program in Quantitative and Computational Biology, Princeton University, Princeton, NJ, USA.
  • Theesfeld CL; Flatiron Institute, Simons Foundation, New York, NY, USA.
  • Wong AK; Flatiron Institute, Simons Foundation, New York, NY, USA.
  • Yuan Y; Laboratory of Molecular Neuro-Oncology and Howard Hughes Medical Institute, The Rockefeller University, New York, NY, USA.
  • Scheckel C; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.
  • Fak JJ; Flatiron Institute, Simons Foundation, New York, NY, USA.
  • Funk J; Laboratory of Molecular Neuro-Oncology and Howard Hughes Medical Institute, The Rockefeller University, New York, NY, USA.
  • Yao K; Gene Therapy Program, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Tajima Y; Laboratory of Molecular Neuro-Oncology and Howard Hughes Medical Institute, The Rockefeller University, New York, NY, USA.
  • Packer A; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.
  • Darnell RB; Laboratory of Molecular Neuro-Oncology and Howard Hughes Medical Institute, The Rockefeller University, New York, NY, USA.
  • Troyanskaya OG; Flatiron Institute, Simons Foundation, New York, NY, USA.
Nat Genet ; 51(6): 973-980, 2019 06.
Article en En | MEDLINE | ID: mdl-31133750
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma Humano / Predisposición Genética a la Enfermedad / ARN no Traducido / Genómica / Trastorno del Espectro Autista / Aprendizaje Profundo / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma Humano / Predisposición Genética a la Enfermedad / ARN no Traducido / Genómica / Trastorno del Espectro Autista / Aprendizaje Profundo / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos