neuropathologiebasel/cqcase repository overview

CQcase is a Plotly Dash web application for visualizing single-case chromosomal copy number variations (CNVs) from precomputed CQcalc results [https://github.com/neuropathbasel-pub/CQcalc⁠]. It features an intuitive GUI with dropdowns for selecting preprocessing methods, bin sizes, probe intersections, and HUGO genes to highlight. Users can browse anomalies, download interactive HTML plots for WORM-compliant archiving, and share views via URLs. This tool supports clinical and research workflows, integrating with EpiDiP for methylation array data.

For full details, visit our GitHub repositories https://github.com/neuropathbasel-pub/CnQuant⁠ and https://github.com/neuropathbasel-pub/CQcase⁠