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Combining targeted sequencing and ultra-low-pass whole-genome sequencing for accurate somatic copy number alteration detection.
Fu, Junfeng; Guo, Weihua; Yan, Cheng; Lv, Zhenyang; Wang, Yu; Wang, Ze; Fan, Zhe; Lei, Ting.
Afiliação
  • Fu J; Department of Thoracic Surgery, The Second Hospital of Dalian Medical University, No.467 Zhongshan Road, Shahekou District, Dalian, 116000, Liaoning Province, China.
  • Guo W; Genetron Health (Beijing) Co. Ltd., Beijing, 102206, China.
  • Yan C; Genetron Health (Beijing) Co. Ltd., Beijing, 102206, China.
  • Lv Z; Department of Thoracic Surgery, The Second Hospital of Dalian Medical University, No.467 Zhongshan Road, Shahekou District, Dalian, 116000, Liaoning Province, China.
  • Wang Y; Department of Thoracic Surgery, The Second Hospital of Dalian Medical University, No.467 Zhongshan Road, Shahekou District, Dalian, 116000, Liaoning Province, China.
  • Wang Z; Department of Thoracic Surgery, The Second Hospital of Dalian Medical University, No.467 Zhongshan Road, Shahekou District, Dalian, 116000, Liaoning Province, China.
  • Fan Z; Department of Thoracic Surgery, The Second Hospital of Dalian Medical University, No.467 Zhongshan Road, Shahekou District, Dalian, 116000, Liaoning Province, China.
  • Lei T; Department of Thoracic Surgery, The Second Hospital of Dalian Medical University, No.467 Zhongshan Road, Shahekou District, Dalian, 116000, Liaoning Province, China. tuohuanyo76@163.com.
Funct Integr Genomics ; 21(2): 161-169, 2021 Mar.
Article em En | MEDLINE | ID: mdl-33543400
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Variações do Número de Cópias de DNA / Carcinogênese / Neoplasias Pulmonares Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Funct Integr Genomics Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China País de publicação: Alemanha
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: Neoplasias Encefálicas / Variações do Número de Cópias de DNA / Carcinogênese / Neoplasias Pulmonares Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Funct Integr Genomics Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China País de publicação: Alemanha