Python and Plotly implementation of an IGV-inspired sequence coverage plot. It efficiently computes sequence coverage from read alignment and provides an interactive visualization annotated with mutations, similar to the Integrative Genome Viewer.

The plots below are interactive (zoom, pan, hover for values). They are hosted on the repo’s GitHub Pages.

Small region of interest (<100 bp)

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Large region of interest (5000 bp)

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View on GitHub →