Towards a European consensus for reporting incidental findings during clinical NGS testing

In 2013, the American College of Medical Genetics (ACMG) examined the issue of incidental findings in whole exome and whole genome sequencing, and introduced recommendations to search for, evaluate and report medically actionable variants in a set of 56 genes. At a debate held during the 2014 Europe...

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Detalhes bibliográficos
Publicado no:Eur J Hum Genet
Main Authors: Hehir-Kwa, Jayne Y, Claustres, Mireille, Hastings, Ros J, van Ravenswaaij-Arts, Conny, Christenhusz, Gabrielle, Genuardi, Maurizio, Melegh, Béla, Cambon-Thomsen, Anne, Patsalis, Philippos, Vermeesch, Joris, Cornel, Martina C, Searle, Beverly, Palotie, Aarno, Capoluongo, Ettore, Peterlin, Borut, Estivill, Xavier, Robinson, Peter N
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2015
Assuntos:
Meeting Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4795187/
https://ncbi.nlm.nih.gov/pubmed/26036857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.111
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