The effects of genomic germline variant reclassification on clinical cancer care

The last two decades have provided an astounding amount of novel information about the human genome. Translating germline genomic data into clinically actionable findings is reliant on the annotation and laboratory classification of specific variants. Variant classification helps providers and patie...

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Detalles Bibliográficos
Autores principales: Slavin, Thomas P., Manjarrez, Sophia, Pritchard, Colin C., Gray, Stacy, Weitzel, Jeffrey N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
Materias:
Research Perspective
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355179/
https://www.ncbi.nlm.nih.gov/pubmed/30728895
http://dx.doi.org/10.18632/oncotarget.26501

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355179/
https://www.ncbi.nlm.nih.gov/pubmed/30728895
http://dx.doi.org/10.18632/oncotarget.26501

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