CytoSure™ Molecular Arrays
Reliable detection of copy number changes for research into a range of genetic disorders. CytoSure Molecular Arrays are designed to accurately identify small intragenic copy number variations (CNVs) in genes associated with a variety of disorders. The content for each array has been designed and optimised in collaboration with leading molecular genetics experts at Emory University. In addition to pre-designed catalogue arrays…
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Reliable detection of copy number changes for research into a range of genetic disorders.
CytoSure Molecular Arrays are designed to accurately identify small intragenic copy number variations (CNVs) in genes associated with a variety of disorders. The content for each array has been designed and optimised in collaboration with leading molecular genetics experts at Emory University. In addition to pre-designed catalogue arrays, you can also utilise our extensive array design expertise to produce custom arrays matching your precise specifications.
CytoSure™ Molecular Arrays Features:
- Accurate detection of copy number variation — a perfect complement to sequencing analysis
- Array content fully optimised and research-validated by Emory University
- Flexible array content and formats — create the ideal array for your needs
- Cost-effective processing — multiple molecular disorders can be included in a single array
- Easy data interpretation using optimised protocols and industry-leading CytoSure Interpret Software
