Comparative Genomic Hybridization
With array CGH or CNV (Copy Number Variant), you can access to a molecular cytogenetic technique with a higher resolution. It is becoming an essential diagnostic tool to detect chromosomal regions lost or gained in tumors for cancer classification or for genomic aberrations identification.
Helixio proposes a CGH/CNV service with Agilent technologies: our numerous collaborations with public or private laboratories are the best demonstration of the recognized know-how of our team concerning array CGH based studies.
A standardized approach for the most common species (human, rat, mouse) is proposed: several high resolution are available from 100 000 to 1 million probes.
A custom approach is available for other species and/or to target regions of interest (genes, chromosomes…). A custom array CGH is designed with Agilent’s SureDesign application according to your specifications.