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Mapping Nucleotide Sequences that Encode Complex Binary Disease Traits with HapMap
Detecting the patterns of DNA sequence variants across the human genome is a crucial step for unraveling the genetic basis of complex human diseases. The human HapMap constructed by single nucleotide polymorphisms (SNPs) provides efficient sequence variation information that can speed up the discove...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Bentham Science Publishers Ltd.
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2652402/ https://ncbi.nlm.nih.gov/pubmed/19384427 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/138920207782446188 |
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