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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korea Genome Organization
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944048/ https://www.ncbi.nlm.nih.gov/pubmed/31896247 http://dx.doi.org/10.5808/GI.2019.17.4.e47 |