Webinar: Analysis of Genome-wide Genotyping Data for Copy Number Variation in Breast Cancer

December 3, 2008, 9:00 AM (PST)

Abstract:

Altered copy number of genes and regulatory regions of the genome can affect human health. Analysis of copy number variation (CNV) is of interest in the context of cancer research. High-density single nucleotide polymorphism (SNP) arrays generate intensity based data which can be analyzed for CNV. Using intensity data from Affymetrix^® SNP arrays, CNV was assessed for breast cancer samples. Data were imported into the Syllego system and analyzed for CNV. Results were stored in the Syllego database and evaluated with built-in data viewers. The workshop will discuss the results of this analysis and how the Syllego system simplifies transfer, visualization, interpretation, and sharing of data with colleagues.

Register now for 9:00 AM Webinar.

Can't make the 9:00 AM Webinar? Register now for the 4:00 PM Webinar.