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Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants.
Przybyla, Weronika; Gjersvoll Paulsen, Kirsti Marie; Mishra, Charitra Kumar; Nygård, Ståle; Engebretsen, Solveig; Ruud, Ellen; Trøen, Gunhild; Beiske, Klaus; Baumbusch, Lars Oliver.
Afiliação
  • Przybyla W; Department of Pediatric Research, Division of Paediatric and Adolescent Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.
  • Gjersvoll Paulsen KM; Medical Faculty, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Mishra CK; Department of Pediatric Research, Division of Paediatric and Adolescent Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.
  • Nygård S; Medical Faculty, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Engebretsen S; Bioinformatics Core Facility, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
  • Ruud E; ELIXIR-Norway, Institute of Informatics, University of Oslo, Oslo, Norway.
  • Trøen G; ELIXIR-Norway, Institute of Informatics, University of Oslo, Oslo, Norway.
  • Beiske K; Norwegian Computing Center, Oslo, Norway.
  • Baumbusch LO; Medical Faculty, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
PLoS One ; 17(8): e0273280, 2022.
Article em En | MEDLINE | ID: mdl-36037157
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variações do Número de Cópias de DNA / Neuroblastoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variações do Número de Cópias de DNA / Neuroblastoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article