Towards Automation of Germline Variant Curation in Clinical Cancer Genetics

PURPOSE: Cancer care professionals are confronted with interpreting results from multiplexed gene sequencing of patients at hereditary risk for cancer. Assessments for variant classification now require orthogonal data searches and aggregation of multiple lines of evidence from diverse resources. Th...

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Detalles Bibliográficos
Autores principales: Ravichandran, Vignesh, Shameer, Zarina, Kemel, Yelena, Walsh, Michael, Cadoo, Karen, Lipkin, Steven, Mandelker, Diana, Zhang, Liying, Stadler, Zsofia, Robson, Mark, Offit, Kenneth, Joseph, Vijai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6703969/
https://www.ncbi.nlm.nih.gov/pubmed/30787465
http://dx.doi.org/10.1038/s41436-019-0463-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6703969/
https://www.ncbi.nlm.nih.gov/pubmed/30787465
http://dx.doi.org/10.1038/s41436-019-0463-8

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