Detection of copy number variations from NGS data using read depth information: a diagnostic performance evaluation
Olivier Quenez(Inserm), Gaël Nicolas(Inserm), Isabelle Tournier(Biotherapy of Genetic Diseases, Inflammatory Disorders and Cancers), Nathalie Le Meur(Établissement Français du Sang), François Lecoquierre(Inserm), Edwige Kasper(Inserm), Thierry Frébourg(Inserm), Gaëlle Bougeard(Inserm), Anne-claire Richard(Biotherapy of Genetic Diseases, Inflammatory Disorders and Cancers), Stéphanie Baert‐Desurmont, Emilie Bouvignies(Inserm), Sophie Coutant(Inserm), Gwendoline Lienard(Inserm), Kilan Le Guennec(Inserm), Stéphanie Vasseur(Inserm), Virginie Nguyen-Viet(Inserm), Kévin Cassinari(Université de Pau et des Pays de l'Adour), Anne Boland(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Géraldine Joly Helas(Centre Hospitalier Universitaire de Rouen), Pascal Chambon(Université de Pau et des Pays de l'Adour), Myriam Vézain(Inserm), Steeve Fourneaux(Inserm), Mathieu Castelain(Inserm), Sandrine Manase(Inserm), Anne Rovelet‐Lecrux(Inserm), Jacqueline Bou(Inserm), Stéphane Rousseau(Inserm), Dominique Campion(Inserm), Jean‐François Deleuze(Fondation Jean Dausset-CEPH), Nathalie Drouot(Centre National de la Recherche Scientifique), Françoise Charbonnier(Inserm), Pascale Saugier-Véber(Inserm)
Unknown
October 16, 2019
Cited by 0
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