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Orphan Diseases
Orphan Disease Database [A-A]
Orphan Disease Database [B-C]
Orphan Disease Database [D-F]
Orphan Disease Database [G-H]
Orphan Disease Database [I-L]
Orphan Disease Database [M-N]
Orphan Disease Database [O-Q]
Orphan Disease Database [R-S]
Orphan Disease Database [T-U]
Orphan Disease Database [W-W]
Orphan Disease Database [X-Z]
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Diagnostics - Orphan Disease Analysis

Orphan Diseases

Arrayit offers the market's first service dedicated exclusively to elucidating orphan human diseases. Orphan (rare) diseases are conditions presenting in a small percentage of the population, typically from 1 in 1,000-200,000 persons. More than 3,100 orphan diseases have been identified but in many cases the molecular details are poorly understood. We deploy our patented and proprietary microarray platform on a genomic scale to elucidate the molecular basis of any orphan disease quickly and efficiently. Control and test samples of mRNA are compared to produce a gene expression signature for each disease. Gene expression data are then examined computationally using advanced mathematics to produce a "best-fit" biological pathway. The sensitivity and specificity of our microarray platform enables a deeper examination of the transcriptome than competing platforms and a more complete understanding of orphan diseases. Genotyping and proteomic analyses are also available to confirm and extend each analysis. Please contact us by electronic mail to learn more about our orphan disease analysis capabilities.
Orphan Disease Database