DNAprint Genomics (DNAG)

[IVRT]

Array design

The foundation for the PHENOMETM system is our unique DNA
databank and SNP database. Our DNA databank couples consent
qualified DNA samples with extensive biographical data for each
sample for broad application to many project types. Our SNP
database is a proprietary assemblage of heretofore unknown and
undocumented SNPs, focused on candidate genes and genetic
pathways known to be involved in a wide variety of biological
functions. Each SNP in our database is linked to 35 different
qualitative and quantitative variables for convenient clustering. Over
70% of the SNPs in our database have not yet been reported in the
literature and do not appear in public databases. When selecting a
custom array of SNPs for your high-throughput needs, we can use
medline accession number, gene names, author names, dates,
population frequencies, various key words (such as cancer,
prostate, xenobiotic) or nucleotide sequences as search subjects for
our database. The goal is to merge information content value with
function based selection routines.

If you’d like to discuss your particular needs with us further,
please contact us at 1877-DNA-FILE.


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