| Literature DB >> 12083399 |
Arnold Oliphant1, David L Barker, John R Stuelpnagel, Mark S Chee.
Abstract
The Human Genome Project has opened the door to personalized medicine, provided that human genetic diversity can be analyzed in a high-throughput and cost-effective way Illumina has developed a genotyping system that combines very high throughput and accuracy with low cost per SNP analysis. The system uses our BeadArray platform, a high level of multiplexing, and modular, scalable automation to meet the requirements for cost-effective, genome-wide linkage disequilibrium studies. As implemented in a high-throughput genotyping service facility at Illumina, the system has a current capacity of one million SNP assays per day and is easily expandable. Each SNP call is associated with a quality score that correlates with accuracyEntities:
Mesh:
Year: 2002 PMID: 12083399
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993