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A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays
Sequencing-based genetic tests to identify individuals at increased risk of hereditary breast and ovarian cancers have resulted in the identification of more than 40,000 sequence variants of BRCA1 and BRCA2. A majority of these variants are considered to be variants of uncertain significance (VUS) b...
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| Pubblicato in: | NPJ Genom Med |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group UK
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7722754/ https://ncbi.nlm.nih.gov/pubmed/33293522 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41525-020-00158-5 |
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