DNAprint Genomics (DNAG)

[IVRT]

PhenomeTM SNiP databases
We have developed unique and comprehensive SNP databases through the use of proprietary, protocols and data mining techniques. At present, we are sequencing 1,000,000 bases of DNA per week. This rate of sequencing has allowed us to discover about 1 novel, quality validated SNP for every 200 bases of target sequence in the human genome. This rate of discovery is greater than that which others have reported in the scientific literature. In contrast to maps present in public resources, the proprietary SNP maps the company is building span the entire length of each target gene. Relatively few of the SNPs comprising these maps are present in public genome database resources. In addition, analysis conducted to date has validated these SNPs (as real polymorphisms) at a significantly higher rate than those taken or "mined" from public database resources. The Company attributes these desirable outcomes to its implementation of unique vertical re-sequencing protocols and proprietary software platform (the patent pending SNiPdoc(tm) system) for raw SNP discovery.

http://www.dnaprint.com./index.cfm?fuseaction=content&id=27