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{{Bioinformatics application
|sw summary=Copy number analysis for exome-sequencing / targeted-resequencing. Two methods of analysis available: Case vs Control, or Case vs Baseline. Function available for creating a baseline from multiple samples. INPUT=BAM files.|bio domain=Next Generation Sequencing, Cancer biology, Genomics|bio method=, Copy number estimation, Copy number analysis, CNV
|bio tech=Illumina
|created by=Jason Li
|created at=Peter MacCallum Cancer Centre, East Melbourne VIC 3002, Australia
|maintained=Yes
|input format=BAM, BED, |output format=VCF, Tab-delimited,
|sw feature=Copy number analysis, baseline (pseudo-control) creation
|language=Python, R
|library=BEDtools, SAMtools
|licence=GPL v3GPLv3, |os=Linux 64, Linux,
}}
== Description ==