Tom Downey demonstrates how Partek® Genomics Suite Version 6.3 can perform interactive primary and secondary copy number analyses for the SNP Arrays 6.0.  He illustrates how researchers who are conducting whole-genome association studies can use the Partek® Genomics Suite to enable automatic detection of copy number changes for known and de novo CNV regions. He also discusses how it enables whole-genome copy number estimation using built-in or user-defined reference sets, including allele-specific analysis, and how it permits automatic detection of regions of LOH.

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