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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...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2011
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| Pynciau: | |
| Mynediad Ar-lein: | 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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