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Detecting rare variants for complex traits using family and unrelated data
Large genome-wide association studies have been performed to detect common genetic variants involved in common diseases, but most of the variants found this way account for only a small portion of the trait variance. Furthermore, candidate gene based resequencing suggests that many rare genetic vari...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2811752/ https://ncbi.nlm.nih.gov/pubmed/19847924 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.20449 |
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