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Detecting Multiethnic Rare Variants
Genome-wide association studies have identified many common genetic variants which are associated with certain diseases. The identified common variants, however, explain only a small portion of the heritability of a complex disease phenotype. The missing heritability motivated researchers to test th...
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| Veröffentlicht in: | Methods Mol Biol |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6350776/ https://ncbi.nlm.nih.gov/pubmed/28980263 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4939-7274-6_26 |
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