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Summarizing polygenic risks for complex diseases in a clinical whole genome report
PURPOSE: Disease-causing mutations and pharmacogenomic variants are of primary interest for clinical whole-genome sequencing. However, estimating genetic liability for common complex diseases using established risk alleles might one day prove clinically useful. METHODS: We compared polygenic scoring...
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| Publicat a: | Genet Med |
|---|---|
| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4547452/ https://ncbi.nlm.nih.gov/pubmed/25341114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2014.143 |
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