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Text replace - "Structural variants" to "Structural variation"
{{Bioinformatics application
|sw summary=We present a novel approach, called CNAseg, to identify CNAs from second-generation sequencing data. It uses depth of coverage to estimate copy number states and flowcell-to-flowcell variability in cancer and normal samples to control the false positive rate.
|bio domain=Structural variantsvariation
|created at=Cancer Research UK Cambridge Research Institute
}}
