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Simple and Efficient Analysis of Disease Association with Missing Genotype Data
Missing genotype data arise in association studies when the single-nucleotide polymorphisms (SNPs) on the genotying platform are not assayed successfully, when the SNPs of interest are not on the platform, or when total sequence variation is determined only on a small fraction of individuals. We pre...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society of Human Genetics
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2427170/ https://ncbi.nlm.nih.gov/pubmed/18252224 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2007.11.004 |
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