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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...
| Autores principales: | , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Bentham Science Publishers Ltd.
2007
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2652402/ https://www.ncbi.nlm.nih.gov/pubmed/19384427 http://dx.doi.org/10.2174/138920207782446188 |