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Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants
BACKGROUND: Clinical laboratories implement a variety of measures to classify somatic sequence variants and identify clinically significant variants to facilitate the implementation of precision medicine. To standardize the interpretation process, the Association for Molecular Pathology (AMP), Ameri...
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| Publicado no: | Genome Med |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6708137/ https://ncbi.nlm.nih.gov/pubmed/31443733 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-019-0664-4 |
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