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A Computational Method to Classify Variants of Uncertain Significance Using Functional Assay Data With Application to BRCA1
BACKGROUND: Besides revealing cancer–predisposition variants or the absence of any changes, genetic testing for cancer predisposition genes can also identify variants of uncertain clinical significance (VUS). Classifying VUSs is a pressing problem as ever more patients seek genetic testing for disea...
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| Главные авторы: | , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2011
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3111818/ https://ncbi.nlm.nih.gov/pubmed/21447777 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1055-9965.EPI-10-1214 |
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