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SNPstream ® UHT: Ultra-High Throughput SNP Genotyping for Pharmacogenomics and Drug Discovery
Author(s) -
Peter A. Bell,
Surendra Chaturvedi,
Craig A. Gelfand,
ChingYu Huang,
Michael Kochersperger,
Rafael Kopla,
Frank S. Modica,
Mark Pohl,
Shobha Varde,
Renbin Zhao,
Xiaojian Zhao,
Michael T. Boyce-Jacino
Publication year - 2002
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/jun0205
Subject(s) - pharmacogenomics , genotyping , drug discovery , snp genotyping , snp , computational biology , biology , genetics , genotype , bioinformatics , single nucleotide polymorphism , gene
Single nucleotide polymorphism (SNP) genotyping is playing an increasing role in genome mapping, pharmacogenetic studies, and drug discovery. To date, genome-wide scans and studies involving thousands of SNPs and samples have been hampered by the lack of a system that can perform genotyping with cost-effective throughput, accuracy, and reliability. To address this need, Orrhid has developed an automated, ultra-high throughput system, SNPstream UHT, which uses multiplexed PCR in conjunction with our next generation SNP-IT tag array single base extension genotyping technology The system employs oligonucleotide microarrays manufactured in a 384-well format on a novel glass-bottomed plate. Multiplexed PCR and genotyping are performed in homogeneous reactions, and assay results are read by direct two-color fluorescence on the SNPstream UHTArray Imager. The systems flexibility enables large projects involving thousands of SNPs and thousands of samples as well as small projects that have hundreds of SNPs and hundreds of samples to be done cost effectively. We have successfully demonstrated this system in greater than 1,000,000 genotyping assays with >96% of samples giving genotypes with >99% accuracy

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