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SNP identification in unamplified human genomic DNA with gold nanoparticle probes
Single nucleotide polymorphisms (SNPs) comprise the most abundant source of genetic variation in the human genome. SNPs may be linked to genetic predispositions, frank disorders or adverse drug responses, or they may serve as genetic markers in linkage disequilibrium analysis. Thus far, established...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC548375/ https://ncbi.nlm.nih.gov/pubmed/15659576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gni017 |
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