Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants

BACKGROUND: Clinical laboratories implement a variety of measures to classify somatic sequence variants and identify clinically significant variants to facilitate the implementation of precision medicine. To standardize the interpretation process, the Association for Molecular Pathology (AMP), Ameri...

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Detalles Bibliográficos
Autores principales: He, Max M., Li, Quan, Yan, Muqing, Cao, Hui, Hu, Yue, He, Karen Y., Cao, Kajia, Li, Marilyn M., Wang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708137/
https://www.ncbi.nlm.nih.gov/pubmed/31443733
http://dx.doi.org/10.1186/s13073-019-0664-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708137/
https://www.ncbi.nlm.nih.gov/pubmed/31443733
http://dx.doi.org/10.1186/s13073-019-0664-4

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