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Application of Machine Learning to Development of Copy Number Variation-based Prediction of Cancer Risk
In the present study, recurrent copy number variations (CNVs) from non-tumor blood cell DNAs of Caucasian non-cancer subjects and glioma, myeloma, and colorectal cancer-patients, and Korean non-cancer subjects and hepatocellular carcinoma, gastric cancer, and colorectal cancer patients, were found t...
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| Publicat a: | Genomics Insights |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Libertas Academica
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4504076/ https://ncbi.nlm.nih.gov/pubmed/26203258 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/GEI.S15002 |
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