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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971104/
https://www.ncbi.nlm.nih.gov/pubmed/33711922
http://dx.doi.org/10.1186/s12859-021-04060-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971104/
https://www.ncbi.nlm.nih.gov/pubmed/33711922
http://dx.doi.org/10.1186/s12859-021-04060-4

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