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Variations in predicted risks in personal genome testing for common complex diseases
PURPOSE: The promise of personalized genomics for common complex diseases depends, in part, on the ability to predict genetic risks on the basis of single nucleotide polymorphisms. We examined and compared the methods of three companies (23andMe, deCODEme, and Navigenics) that have offered direct-to...
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| Main Authors: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2013
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3883880/ https://ncbi.nlm.nih.gov/pubmed/23807614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2013.80 |
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