Somatic cancer variant curation and harmonization through consensus minimum variant level data

BACKGROUND: To truly achieve personalized medicine in oncology, it is critical to catalog and curate cancer sequence variants for their clinical relevance. The Somatic Working Group (WG) of the Clinical Genome Resource (ClinGen), in cooperation with ClinVar and multiple cancer variant curation stake...

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Detalles Bibliográficos
Autores principales: Ritter, Deborah I., Roychowdhury, Sameek, Roy, Angshumoy, Rao, Shruti, Landrum, Melissa J., Sonkin, Dmitriy, Shekar, Mamatha, Davis, Caleb F., Hart, Reece K., Micheel, Christine, Weaver, Meredith, Van Allen, Eliezer M., Parsons, Donald W., McLeod, Howard L., Watson, Michael S., Plon, Sharon E., Kulkarni, Shashikant, Madhavan, Subha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095986/
https://www.ncbi.nlm.nih.gov/pubmed/27814769
http://dx.doi.org/10.1186/s13073-016-0367-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095986/
https://www.ncbi.nlm.nih.gov/pubmed/27814769
http://dx.doi.org/10.1186/s13073-016-0367-z

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