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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...
Autores principales: | Slavin, Thomas P., Manjarrez, Sophia, Pritchard, Colin C., Gray, Stacy, Weitzel, Jeffrey N. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2019
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Materias: | |
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 |
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