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Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiers

Abstract Background Recently, copy number variations (CNV) impacting genes involved in oncogenic pathways have attracted an increasing attention to manage disease susceptibility. CNV is one of the most important somatic aberrations in the genome of tumor cells. Oncogene activation and tumor suppress...

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Autors principals: Pierre-Julien Viailly, Vincent Sater, Mathieu Viennot, Elodie Bohers, Nicolas Vergne, Caroline Berard, Hélène Dauchel, Thierry Lecroq, Alison Celebi, Philippe Ruminy, Vinciane Marchand, Marie-Delphine Lanic, Sydney Dubois, Dominique Penther, Hervé Tilly, Sylvain Mareschal, Fabrice Jardin
Format: Artigo
Idioma:Inglês
Publicat: BMC 2021-03-01
Col·lecció:BMC Bioinformatics
Matèries:
UMI
CNV calling
Next generation sequencing
Accés en línia:https://doi.org/10.1186/s12859-021-04060-4
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