BBCAnalyzer: a visual approach to facilitate variant calling

BACKGROUND: Deriving valid variant calling results from raw next-generation sequencing data is a particularly challenging task, especially with respect to clinical diagnostics and personalized medicine. However, when using classic variant calling software, the user usually obtains nothing more than...

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Detalles Bibliográficos
Autores principales: Sandmann, Sarah, de Graaf, Aniek O., Dugas, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330023/
https://www.ncbi.nlm.nih.gov/pubmed/28241736
http://dx.doi.org/10.1186/s12859-017-1549-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330023/
https://www.ncbi.nlm.nih.gov/pubmed/28241736
http://dx.doi.org/10.1186/s12859-017-1549-4

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