🧬 Read Mapping and Variant Calling Lab: Coverage, Error Rate and Missed Mutations

Sequence a synthetic genome, map the reads, pile them up and call single-base variants. Move coverage, read length, error rate and the QUAL threshold and watch recall and precision change on a 3D DNA bench, with a Lander-Waterman depth histogram, a Smith-Waterman explorer and independent numerical checks.

3D · Three.js / WebGL renderer · 60 FPS target · runs fully client-side, no install