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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Eur J Hum Genet
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2015
Pynciau:
Meeting Report
Mynediad Ar-lein: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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