Diagnose with confidence. Defensible at every step.

Coverage plots display chromosome-specific read depth, making large structural variants immediately visible. Scan the genome at a glance (similar to karyotyping) to spot deletions, duplications, and other large-scale events before drilling into the detailed variant view.

Map the entire genome in a circular layout, with arcs connecting distant loci to reveal translocations and other inter-chromosomal rearrangements at a glance. Trace structural connections across chromosomes, including fusions, balanced translocations, and complex rearrangements.

Phenotype-driven variant prioritization ranks candidate variants against the patient's clinical presentation, surfacing the most likely causal variants first. Enter HPO terms and Lucid weighs each variant by gene-phenotype association, narrowing thousands of candidates to a focused shortlist before you begin detailed review.

Phenotype Match visually highlights which variants fall in genes linked to the patient's HPO terms, making the overlap between candidate variants and phenotype-associated genes immediately clear at a glance.

Advanced filtering lets you combine criteria, allele frequency, inheritance pattern, variant type, ACMG class, gene panels, and more to narrow candidates to exactly the set you want to review.

Lucid provides detailed variant visualizations that go beyond the standard sequence view, including epigenetic tracks and topologically associating domain (TAD) boundaries. See how variants sit within their regulatory context, from methylation signatures to chromatin architecture, revealing functional impact that base-level analysis alone can miss.