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Lucid Genomics

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  • Product title:
    Lucid Genome Suite
    Product description:

    Lucid Genomics is a cloud-native secondary and tertiary analysis platform built from the ground up for long-read sequencing. We develop dedicated products for rare disease diagnostics, hereditary cancer, and pharmacogenomics. As nanopore sequencing scales, the real opportunity lies in uncovering what was previously invisible: structural variants, methylation patterns, repeat expansions, and dark genome regions. Lucid is a pioneer in long-read interpretation, combining proprietary prioritization algorithms with cutting-edge visualizations purpose-built for long-read data. Together with native variant calling, advanced phasing, and annotation, this delivers a validated path from sequencer to actionable insights. As trusted Oxford Nanopore partner, Lucid helps Clinical Labs, Researchers and Pharma innovators to realize the full promise of long-read genomics.

    Specific use application:
    Rare Disease, Pharmacogenomics, Hereditary Cancer
    Territory:
    Worldwide

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