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Pure additive contribution of genetic variants to a risk prediction model using propensity score matching: application to type 2 diabetes
The achievements of genome-wide association studies have suggested ways to predict diseases, such as type 2 diabetes (T2D), using single-nucleotide polymorphisms (SNPs). Most T2D risk prediction models have used SNPs in combination with demographic variables. However, it is difficult to evaluate the...
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| Publicado no: | Genomics Inform |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korea Genome Organization
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6944048/ https://ncbi.nlm.nih.gov/pubmed/31896247 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5808/GI.2019.17.4.e47 |
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