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Genomic variant annotation workflow for clinical applications
Annotation and interpretation of DNA aberrations identified through next-generation sequencing is becoming an increasingly important task. Even more so in the context of data analysis pipelines for medical applications, where genomic aberrations are associated with phenotypic and clinical features....
Autores principales: | Thurnherr, Thomas, Singer, Franziska, Stekhoven, Daniel J., Beerenwinkel, Niko |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5130070/ https://www.ncbi.nlm.nih.gov/pubmed/27990260 http://dx.doi.org/10.12688/f1000research.9357.2 |
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