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Standardized decision support in next generation sequencing reports of somatic cancer variants
Of hundreds to thousands of somatic mutations that exist in each cancer genome, a large number are unique and non‐recurrent variants. Prioritizing genetic variants identified via next generation sequencing technologies remains a major challenge. Many such variants occur in tumor genes that have well...
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發表在: | Mol Oncol |
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Main Authors: | , , , , , , |
格式: | Artigo |
語言: | Inglês |
出版: |
John Wiley and Sons Inc.
2014
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主題: | |
在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5528527/ https://ncbi.nlm.nih.gov/pubmed/24768039 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.molonc.2014.03.021 |
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