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Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing.
Stangl, Christina; de Blank, Sam; Renkens, Ivo; Westera, Liset; Verbeek, Tamara; Valle-Inclan, Jose Espejo; González, Rocio Chamorro; Henssen, Anton G; van Roosmalen, Markus J; Stam, Ronald W; Voest, Emile E; Kloosterman, Wigard P; van Haaften, Gijs; Monroe, Glen R.
Afiliação
  • Stangl C; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht and Utrecht University, Utrecht, Netherlands.
  • de Blank S; Division of Molecular Oncology, Netherlands Cancer Institute, Plesmanlaan, Amsterdam, Netherlands.
  • Renkens I; Oncode Institute, 3521 AL, Utrecht, Netherlands.
  • Westera L; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht and Utrecht University, Utrecht, Netherlands.
  • Verbeek T; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht and Utrecht University, Utrecht, Netherlands.
  • Valle-Inclan JE; Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
  • González RC; Dutch Childhood Oncology Group (DCOG), Den Haag, Netherlands.
  • Henssen AG; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht and Utrecht University, Utrecht, Netherlands.
  • van Roosmalen MJ; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht and Utrecht University, Utrecht, Netherlands.
  • Stam RW; Oncode Institute, 3521 AL, Utrecht, Netherlands.
  • Voest EE; Department of Pediatric Oncology/Hematology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Kloosterman WP; Experimental and Clinical Research Center (ECRC) of the MDC and Charité Berlin, Berlin, Germany.
  • van Haaften G; Department of Pediatric Oncology/Hematology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Monroe GR; Experimental and Clinical Research Center (ECRC) of the MDC and Charité Berlin, Berlin, Germany.
Nat Commun ; 11(1): 2861, 2020 06 05.
Article em En | MEDLINE | ID: mdl-32504042
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Fusão Gênica / Sistemas CRISPR-Cas / Sequenciamento por Nanoporos / Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Fusão Gênica / Sistemas CRISPR-Cas / Sequenciamento por Nanoporos / Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article