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Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiers.
Viailly, Pierre-Julien; Sater, Vincent; Viennot, Mathieu; Bohers, Elodie; Vergne, Nicolas; Berard, Caroline; Dauchel, Hélène; Lecroq, Thierry; Celebi, Alison; Ruminy, Philippe; Marchand, Vinciane; Lanic, Marie-Delphine; Dubois, Sydney; Penther, Dominique; Tilly, Hervé; Mareschal, Sylvain; Jardin, Fabrice.
Afiliação
  • Viailly PJ; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France. pierre-julien.viailly@chb.unicancer.fr.
  • Sater V; Centre Henri Becquerel, Rouen, France. pierre-julien.viailly@chb.unicancer.fr.
  • Viennot M; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.
  • Bohers E; Centre Henri Becquerel, Rouen, France.
  • Vergne N; LITIS EA 4108, Normandie Univ, UNIROUEN, Rouen, France.
  • Berard C; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.
  • Dauchel H; Centre Henri Becquerel, Rouen, France.
  • Lecroq T; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.
  • Celebi A; Centre Henri Becquerel, Rouen, France.
  • Ruminy P; LMRS UMRS 6085, Normandie Univ, UNIROUEN, Rouen, France.
  • Marchand V; LITIS EA 4108, Normandie Univ, UNIROUEN, Rouen, France.
  • Lanic MD; LITIS EA 4108, Normandie Univ, UNIROUEN, Rouen, France.
  • Dubois S; LITIS EA 4108, Normandie Univ, UNIROUEN, Rouen, France.
  • Penther D; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.
  • Tilly H; Centre Henri Becquerel, Rouen, France.
  • Mareschal S; Master Bioinformatique BIM, Normandie Univ, UNIROUEN, Rouen, France.
  • Jardin F; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.
BMC Bioinformatics ; 22(1): 120, 2021 Mar 12.
Article em En | MEDLINE | ID: mdl-33711922
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hibridização Genômica Comparativa / Variações do Número de Cópias de DNA / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Clinical_trials / Observational_studies Limite: Adult / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 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: Hibridização Genômica Comparativa / Variações do Número de Cópias de DNA / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Clinical_trials / Observational_studies Limite: Adult / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article