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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:BMC Bioinformatics
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2021
Pynciau:
Methodology Article
Mynediad Ar-lein: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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