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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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| Publicado no: | BMC Bioinformatics |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5330023/ https://ncbi.nlm.nih.gov/pubmed/28241736 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1549-4 |
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