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QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction.
Deveau, Paul; Colmet Daage, Leo; Oldridge, Derek; Bernard, Virginie; Bellini, Angela; Chicard, Mathieu; Clement, Nathalie; Lapouble, Eve; Combaret, Valerie; Boland, Anne; Meyer, Vincent; Deleuze, Jean-Francois; Janoueix-Lerosey, Isabelle; Barillot, Emmanuel; Delattre, Olivier; Maris, John M; Schleiermacher, Gudrun; Boeva, Valentina.
Afiliação
  • Deveau P; Institut Curie, PSL Research University, Mines Paris Tech, INSERM U900, Paris 75005, France.
  • Colmet Daage L; Département de Recherche Translationnelle, Institut Curie, PSL Research University, INSERM U830, Laboratoire RTOP (Recherche Translationelle en Oncologie Pédiatrique), SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Paris 75005, France.
  • Oldridge D; University of Paris-Sud, Orsay, France.
  • Bernard V; Département de Recherche Translationnelle, Institut Curie, PSL Research University, INSERM U830, Laboratoire RTOP (Recherche Translationelle en Oncologie Pédiatrique), SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Paris 75005, France.
  • Bellini A; Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Chicard M; Center for Childhood Cancer Research Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Clement N; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  • Lapouble E; Institut Curie, PSL Research University, NGS platform ICGex, Paris 75005, France.
  • Combaret V; Département de Recherche Translationnelle, Institut Curie, PSL Research University, INSERM U830, Laboratoire RTOP (Recherche Translationelle en Oncologie Pédiatrique), SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Paris 75005, France.
  • Boland A; Département de Recherche Translationnelle, Institut Curie, PSL Research University, INSERM U830, Laboratoire RTOP (Recherche Translationelle en Oncologie Pédiatrique), SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Paris 75005, France.
  • Meyer V; Département de Recherche Translationnelle, Institut Curie, PSL Research University, INSERM U830, Laboratoire RTOP (Recherche Translationelle en Oncologie Pédiatrique), SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Paris 75005, France.
  • Deleuze JF; Unité de Génétique Somatique, Institut Curie, PSL Research University, Paris 75005, France.
  • Janoueix-Lerosey I; Centre Léon-Bérard Laboratoire de Recherche Translationnelle, Lyon, France.
  • Barillot E; Centre National de Recherche en Génomique Humaine (CNRGH), Institut de biologie François Jacob, CEA, Evry 91057, France.
  • Delattre O; Centre National de Recherche en Génomique Humaine (CNRGH), Institut de biologie François Jacob, CEA, Evry 91057, France.
  • Maris JM; Centre National de Recherche en Génomique Humaine (CNRGH), Institut de biologie François Jacob, CEA, Evry 91057, France.
  • Schleiermacher G; Institut Curie, PSL Research University, INSERM U830, SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Equipe labellisée Ligue Nationale contre le cancer, Paris 75005, France.
  • Boeva V; Institut Curie, PSL Research University, Mines Paris Tech, INSERM U900, Paris 75005, France.
Bioinformatics ; 34(11): 1808-1816, 2018 06 01.
Article em En | MEDLINE | ID: mdl-29342233
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Software / Variações do Número de Cópias de DNA / Tipagem Molecular / Evolução Clonal / Sequenciamento Completo do Genoma / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Bioinformatics Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Software / Variações do Número de Cópias de DNA / Tipagem Molecular / Evolução Clonal / Sequenciamento Completo do Genoma / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Bioinformatics Ano de publicação: 2018 Tipo de documento: Article