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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Publicado en:Genet Med
Main Authors: 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: Artigo
Idioma:Inglês
Publicado: 2019
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6703969/
https://ncbi.nlm.nih.gov/pubmed/30787465
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-019-0463-8
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