Needlestack: an ultra-sensitive variant caller for multi-sample next generation sequencing data

The emergence of next-generation sequencing (NGS) has revolutionized the way of reaching a genome sequence, with the promise of potentially providing a comprehensive characterization of DNA variations. Nevertheless, detecting somatic mutations is still a difficult problem, in particular when trying...

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Detalhes bibliográficos
Publicado no:NAR Genom Bioinform
Main Authors: Delhomme, Tiffany M, Avogbe, Patrice H, Gabriel, Aurélie A G, Alcala, Nicolas, Leblay, Noemie, Voegele, Catherine, Vallée, Maxime, Chopard, Priscilia, Chabrier, Amélie, Abedi-Ardekani, Behnoush, Gaborieau, Valérie, Holcatova, Ivana, Janout, Vladimir, Foretová, Lenka, Milosavljevic, Sasa, Zaridze, David, Mukeriya, Anush, Brambilla, Elisabeth, Brennan, Paul, Scelo, Ghislaine, Fernandez-Cuesta, Lynnette, Byrnes, Graham, Calvez-Kelm, Florence L, McKay, James D, Foll, Matthieu
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2020
Assuntos:
Methart
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7182099/
https://ncbi.nlm.nih.gov/pubmed/32363341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nargab/lqaa021
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