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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....

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Detalles Bibliográficos
Autores principales: Thurnherr, Thomas, Singer, Franziska, Stekhoven, Daniel J., Beerenwinkel, Niko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
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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