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A new disease-specific machine learning approach for the prediction of cancer-causing missense variants
High-throughput genotyping and sequencing techniques are rapidly and inexpensively providing large amounts of human genetic variation data. Single Nucleotide Polymorphisms (SNPs) are an important source of human genome variability and have been implicated in several human diseases, including cancer....
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| Auteurs principaux: | , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2011
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3371640/ https://ncbi.nlm.nih.gov/pubmed/21763417 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ygeno.2011.06.010 |
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