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Detecting association of rare and common variants based on cross-validation prediction error
Despite the extensive discovery of disease-associated common variants, much of the genetic contribution to complex traits remains unexplained. Rare variants may explain additional disease risk or trait variability. Although sequencing technology provides a supreme opportunity to investigate the role...
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| Publicat a: | Genet Epidemiol |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5503115/ https://ncbi.nlm.nih.gov/pubmed/28176359 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.22034 |
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