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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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| Опубликовано в: : | Eur J Hum Genet |
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| Главные авторы: | , , , , , , , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Nature Publishing Group
2015
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| Предметы: | |
| Online-ссылка: | 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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