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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v: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
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2021
Teme:
Methodology Article
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki