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

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 suppressor gene...

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Detalhes bibliográficos
Publicado no:BMC Bioinformatics
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2021
Assuntos:
Methodology Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7971104/
https://ncbi.nlm.nih.gov/pubmed/33711922
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-021-04060-4
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