Events
The February webinar.
Join us in late February to talk about the difficulties of detecting, verifying and genotyping Copy Number Variation in the genome. It's the new frontier for clinically-relevant disease causing variation, and an untapped resevoir of biological information.
Email us at info@igenixinc.com to sign up
The iGenix mission is to provide our clients with the industry's most accurate, timely and affordable research data. Since it's founding in 2007, iGenix has become a leading provider of innovative and customized genomic research solutions, from assaying copy number variation, to methylation and protein detection. We add significant technological expertise and efficiency to your project, meeting the highest expectations.
Our Scientific Expertise 
Success in the lab is directly related to experience. The scientists and technicians at iGenix have extensive experience developing and implementing comprehensive research solutions to yield maximally informative data. The iGenix team has technical expertise in both standard and advanced molecular biology techniques and platforms. We are a leading provider for custom genotyping, copy number variation and other hard-to-type variation as well as methylation and expression study-related services.
Relevant Publications by Our Scientific Staff
High-throughput genotyping of intermediate-size structural variation. Newman-Eerkes TL, et. al. Hum Mol Genet. 2006 Apr 1;15(7):1159-67. Epub 2006 Feb 23.
Mapping and sequencing of structural variation from eight human genomes. Kidd et. al. Nature. 2008. May 1;453(7191):56-64.
Fine-scale structural variation of the human genome. Tuzun E., et. al. Nat Genet. 2005 Jul;37(7):727-32. Epub 2005 May 15.
