ADMIRE is a tool for identification repeated copy number variation (CNV). The ADMIRE algorithm identifies recurrent, multi-scale events, and uses multi-scale Gaussian smoothing. The ADMIRE algorithm does not require segmentation nor calling for the input dataset because it controls the false recovery analytically. The output of the algorithm is a single profile of significant events selected from the scales.
Genetics; Genetic variation
van Dyk E, Reinders MJ, Wessels LF "A scale-space method for detecting recurrent DNA copy number changes with analytical false discovery rate control." Nucleic Acids Res. 2013 May;41(9):e100. https://doi.org/10.1093/nar/gkt155
PMID: 23476020
PMCID: PMC3643574
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