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Fig. 2 | BMC Bioinformatics

Fig. 2

From: ConanVarvar: a versatile tool for the detection of large syndromic copy number variation from whole-genome sequencing data

Fig. 2

Example of the occurrence calculation. ConanVarvar first calculates the Manhattan distance (in bins) between all identified CNVs and creates an adjacency matrix, which is then used to build a graph. Each disconnected component in the graph corresponds to a group of CNVs that are sufficiently close to each other. The occurrence value is then calculated as the number of nodes in each disconnected component

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BMC Bioinformatics

ISSN: 1471-2105

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