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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Détails bibliographiques

Publié dans:	Nucleic Acids Res
Auteurs principaux:	Pickering, Judith, Bamford, Anona, Godbole, Varsha, Briggs, Jackie, Scozzafava, Giuseppe, Roe, Phyllida, Wheeler, Claire, Ghouze, Firman, Cuss, Sarah
Format:	Artigo
Langue:	Inglês
Publié:	Oxford University Press 2002
Sujets:	NAR Methods Online
Accès en ligne:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC117302/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12060698/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/gnf060
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