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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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| Foilsithe in: | Genet Med |
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| Main Authors: | , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2014
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| Ábhair: | |
| Rochtain Ar Líne: | 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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