Parallel Genotyping of Over 10,000 SNPs Using a One-Primer Assay on a High-Density Oligonucleotide Array

The analysis of single nucleotide polymorphisms (SNPs) is increasingly utilizedto investigate the genetic causes of complex human diseases. Here we present a high-throughput genotyping platform that uses a one-primer assay to genotype over 10,000 SNPs per individual on a single oligonucleotide array...

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Detalhes bibliográficos
Main Authors: Matsuzaki, Hajime, Loi, Halina, Dong, Shoulian, Tsai, Ya-Yu, Fang, Joy, Law, Jane, Di, Xiaojun, Liu, Wei-Min, Yang, Geoffrey, Liu, Guoying, Huang, Jing, Kennedy, Giulia C., Ryder, Thomas B., Marcus, Gregory A., Walsh, P. Sean, Shriver, Mark D., Puck, Jennifer M., Jones, Keith W., Mei, Rui
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2004
Assuntos:
Methods
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC353229/
https://ncbi.nlm.nih.gov/pubmed/14993208
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.2014904
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