The present invention relates to genetic analysis and evaluation utilizing copy-number variants or polymorphisms. The methods utilize array comparative genomic hybridization and PCR assays to identify the significance of copy number variations in a subject or subject group.

 
Web www.patentalert.com

< Method, computing routine, device for predicting properties of MHC/peptide complexes, and data and peptides produced therefrom

> Systems and methods for predicting an individual's risk of developing rheumatoid arthritis

> Hypoxia inducible VEGF plasmid for ischemic disease

~ 00598