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Variant information systems for precision oncology

BACKGROUND: The decreasing cost of obtaining high-quality calls of genomic variants and the increasing availability of clinically relevant data on such variants are important drivers for personalized oncology. To allow rational genome-based decisions in diagnosis and treatment, clinicians need intui...

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Detalles Bibliográficos
Autores principales:	Starlinger, Johannes, Pallarz, Steffen, Ševa, Jurica, Rieke, Damian, Sers, Christine, Keilholz, Ulrich, Leser, Ulf
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249891/ https://www.ncbi.nlm.nih.gov/pubmed/30463544 http://dx.doi.org/10.1186/s12911-018-0665-z

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