This repository was developed for the interactive analysis and visualisation of genome-wide copy number variations (CNV) from Whole-Genome-Sequencing (WGS) data using CNVpytor [1].

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1. Suvakov M, Panda A, Diesh C, Holmes I, Abyzov A. CNVpytor: a tool for copy number variation detection and analysis from read depth and allele imbalance in whole-genome sequencing. GigaScience. 2021 Nov 1;10(11):giab074. https://doi.org/10.1093/gigascience/giab074