It's a data analysis tool with detection of genome-wide copy number changes.
Main Features:
-From alignment of raw data to categorization and annotation of mutations in three simple steps
-Supports four different types of analysis: Single Sample, Tumor-Normal, Trio and OneSeq CNV and Mutation Analysis
-Supports variant annotation from many public sources, including NCBI, COSMIC, PubMed, ClinVar and custom annotation
-Reduces time-to-results from days to hours without complex IT infrastructure or special hardware
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