NextGENe Online Help : NextGENe Viewer Comparison Reports and Tools : The CNV (Copy Number Variation) Tool
The CNV (Copy Number Variation) Tool
You generate a CNV Tool report to detail the parallel comparisons of the copy number variations in projects that were aligned independently to the same reference sequence. One project file must be the sample and all other project files must be the control. Two methods are available for comparing the copy number variation: Dispersion and HMM or SNP-based Normalization with smoothing.