Scanning and Data Analysis for Investigating Genomic Copy Number Imbalance

This webinar aired on March 24, 2009

Presenters

• Varshal Dave, Marketing Director, Molecular Devices
• Tony Lialin, Director of North American Sales, BlueGnome
• Yvonne Beirne FitzGerald, Field Application Scientist, Molecular Devices

Learn about the leading solutions for detection of copy number variations in the human genome, which allows for the elucidation of genetic disease, investigation of hematological malignancies and aneuploidy screening of single cells.  Hear how to read the highest quality research use only microarray slides on the Axon family of microarray scanners which have long been hailed as the industry leader in performance, features, and ease-of-use. 

Join speakers form Molecular Devices and BlueGnome for an introduction to ArrayCGH  and Cytochips and Molecular Devices Axon Microarray Scanners.

Topics

• Solutions for detection of copy number variation in the human genome
• Open Platform approach to microarray analysis
• Enhancements to the software enabling data analysis
• Working with Molecular Devices Axon Scanners and the BlueGnome BlueFuse Software

Replay coming soon.