appreci8: a pipeline for precise variant calling integrating 8 tools

MOTIVATION: The application of next-generation sequencing in research and particularly in clinical routine requires valid variant calling results. However, evaluation of several commonly used tools has pointed out that not a single tool meets this requirement. False positive as well as false negativ...

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Detalhes bibliográficos
Publicado no:Bioinformatics
Main Authors: Sandmann, Sarah, Karimi, Mohsen, de Graaf, Aniek O, Rohde, Christian, Göllner, Stefanie, Varghese, Julian, Ernsting, Jan, Walldin, Gunilla, van der Reijden, Bert A, Müller-Tidow, Carsten, Malcovati, Luca, Hellström-Lindberg, Eva, Jansen, Joop H, Dugas, Martin
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
Assuntos:
Original Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6289140/
https://ncbi.nlm.nih.gov/pubmed/29945233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty518
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