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Methodology for the analysis of rare genetic variation in genome-wide association and re-sequencing studies of complex human traits
Genome-wide association studies have been successful in identifying common variants that impact complex human traits and diseases. However, despite this success, the joint effects of these variants explain only a small proportion of the genetic variance in these phenotypes, leading to speculation th...
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| Main Authors: | , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Oxford University Press
2014
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4168660/ https://ncbi.nlm.nih.gov/pubmed/24916163 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bfgp/elu012 |
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