Integration of DNA ligation and rolling circle amplification for the homogeneous, end-point detection of single nucleotide polymorphisms

Association studies using common sequence variants or single nucleotide polymorphisms (SNPs) may provide a powerful approach to dissect the genetic inheritance of common complex traits. Such studies necessitate the development of cost-effective, high throughput technologies for scoring SNPs. The met...

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Autori principali: Pickering, Judith, Bamford, Anona, Godbole, Varsha, Briggs, Jackie, Scozzafava, Giuseppe, Roe, Phyllida, Wheeler, Claire, Ghouze, Firman, Cuss, Sarah
Natura: Articolo
Lingua:en
Pubblicazione: Oxford University Press 2002
Soggetti:
NAR Methods Online
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC117302/
https://ncbi.nlm.nih.gov/pubmed/12060698
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https://ncbi.nlm.nih.gov/pmc/articles/PMC117302/
https://ncbi.nlm.nih.gov/pubmed/12060698

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