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Optimal Haplotype Block-Free Selection of Tagging SNPs for Genome-Wide Association Studies
It is widely hoped that the study of sequence variation in the human genome will provide a means of elucidating the genetic component of complex diseases and variable drug responses. A major stumbling block to the successful design and execution of genome-wide disease association studies using singl...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC509273/ https://ncbi.nlm.nih.gov/pubmed/15289481 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.2570004 |
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