Challenges to Building a Gene Variant Commons to Assess Hereditary Cancer Risk: Results of a Modified Policy Delphi Panel Deliberation

Understanding the clinical significance of variants associated with hereditary cancer risk requires access to a pooled data resource or network of resources—a “cancer gene variant commons”—incorporating representative, well-characterized genetic data, metadata, and, for some purposes, pathways to ca...

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Detalles Bibliográficos
Autores principales: Majumder, Mary A., Blank, Matthew L., Geary, Janis, Bollinger, Juli M., Guerrini, Christi J., Robinson, Jill Oliver, Canfield, Isabel, Cook-Deegan, Robert, McGuire, Amy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305920/
https://www.ncbi.nlm.nih.gov/pubmed/34357113
http://dx.doi.org/10.3390/jpm11070646

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305920/
https://www.ncbi.nlm.nih.gov/pubmed/34357113
http://dx.doi.org/10.3390/jpm11070646

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