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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Detalles Bibliográficos
Autores principales: Bao, Y. Paul, Huber, Martin, Wei, Tai-Fen, Marla, Sudhakar S., Storhoff, James J., Müller, Uwe R.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548375/
https://www.ncbi.nlm.nih.gov/pubmed/15659576
http://dx.doi.org/10.1093/nar/gni017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548375/
https://www.ncbi.nlm.nih.gov/pubmed/15659576
http://dx.doi.org/10.1093/nar/gni017

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