Your browser doesn't support javascript.
loading
Detection of chromosome structural variation by targeted next-generation sequencing and a deep learning application.
Park, Hosub; Chun, Sung-Min; Shim, Jooyong; Oh, Ji-Hye; Cho, Eun Jeong; Hwang, Hee Sang; Lee, Ji-Young; Kim, Deokhoon; Jang, Se Jin; Nam, Soo Jeong; Hwang, Changha; Sohn, Insuk; Sung, Chang Ohk.
Afiliação
  • Park H; Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Chun SM; Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Shim J; Center for Cancer Genome Discovery, Asan Institute for Life Science, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Oh JH; Institute of Statistical Information, Department of Statistics, Inje University, Gyeongsangnam-do, Korea.
  • Cho EJ; Department of Medical Science, Asan Medical Institute of Convergence Science and Technology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Hwang HS; Department of Medical Science, Asan Medical Institute of Convergence Science and Technology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Lee JY; Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Kim D; Center for Cancer Genome Discovery, Asan Institute for Life Science, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Jang SJ; Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Nam SJ; Center for Cancer Genome Discovery, Asan Institute for Life Science, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Hwang C; Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Sohn I; Center for Cancer Genome Discovery, Asan Institute for Life Science, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Sung CO; Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
Sci Rep ; 9(1): 3644, 2019 03 06.
Article em En | MEDLINE | ID: mdl-30842562
Assuntos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oligodendroglioma / Cromossomos Humanos Par 1 / Cromossomos Humanos Par 19 / Aberrações Cromossômicas / Estruturas Cromossômicas / Sequenciamento de Nucleotídeos em Larga Escala / Aprendizado Profundo Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2019 Tipo de documento: Article País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oligodendroglioma / Cromossomos Humanos Par 1 / Cromossomos Humanos Par 19 / Aberrações Cromossômicas / Estruturas Cromossômicas / Sequenciamento de Nucleotídeos em Larga Escala / Aprendizado Profundo Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2019 Tipo de documento: Article País de publicação: Reino Unido