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Somatic cancer variant curation and harmonization through consensus minimum variant level data.
Ritter, Deborah I; Roychowdhury, Sameek; Roy, Angshumoy; Rao, Shruti; Landrum, Melissa J; Sonkin, Dmitriy; Shekar, Mamatha; Davis, Caleb F; Hart, Reece K; Micheel, Christine; Weaver, Meredith; Van Allen, Eliezer M; Parsons, Donald W; McLeod, Howard L; Watson, Michael S; Plon, Sharon E; Kulkarni, Shashikant; Madhavan, Subha.
Afiliación
  • Ritter DI; Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
  • Roychowdhury S; Ohio State University, Columbus, OH, USA.
  • Roy A; Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
  • Rao S; Innovation Center for Biomedical Informatics and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, USA.
  • Landrum MJ; National Center for Biotechnology Information, Bethesda, MD, USA.
  • Sonkin D; National Cancer Institute, Rockville, MD, USA.
  • Shekar M; Illumina, San Diego, CA, USA.
  • Davis CF; MolecularMatch, Houston, TX, USA.
  • Hart RK; Invitae, San Francisco, CA, USA.
  • Micheel C; Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Weaver M; American College of Medical Genetics and Genomics, Bethesda, MD, USA.
  • Van Allen EM; Dana-Farber Cancer Institute, Boston, MA, USA.
  • Parsons DW; Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
  • McLeod HL; Moffitt Cancer Center, Tampa, FL, USA.
  • Watson MS; American College of Medical Genetics and Genomics, Bethesda, MD, USA.
  • Plon SE; Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
  • Kulkarni S; Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
  • Madhavan S; Innovation Center for Biomedical Informatics and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, USA. sm696@georgetown.edu.
Genome Med ; 8(1): 117, 2016 11 04.
Article en En | MEDLINE | ID: mdl-27814769
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Curaduría de Datos / Neoplasias Tipo de estudio: Guideline / Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Genome Med Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Curaduría de Datos / Neoplasias Tipo de estudio: Guideline / Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Genome Med Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos