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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Bibliografiska uppgifter
I publikationen:Genet Med
Huvudupphovsmän: Ravichandran, Vignesh, Shameer, Zarina, Kemel, Yelena, Walsh, Michael, Cadoo, Karen, Lipkin, Steven, Mandelker, Diana, Zhang, Liying, Stadler, Zsofia, Robson, Mark, Offit, Kenneth, Joseph, Vijai
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2019
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Article
Länkar: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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