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The Leading Platform for Long Read Genomics

Lucid Genome suite: Your platform for Long-Read and methylation data analysis

Thursday March 26

4:00 PM CET | 10:00 AM EST

Labs have invested heavily in long-read sequencing platforms — yet turning that data into actionable biological insights remains a major challenge.

In this webinar, we’ll showcase the latest features of the Lucid Whole Genome Analysis Platform, designed for intuitive, end-to-end analysis of long-read WGS data.

We look forward to seeing many of you.

New interface

Interface updates will support you in finding your way on the platform as ntuitive and easy as possible

Large Variant Visualization

Chromosome wide coverage plots and circos plots will support you in detection and interpretation of all types of large variants

Differentially Methylated Region Support

We have integrated CpG-level methylation visualization, allele-specific methylation display (if phased data available) and more

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HPO Variant Matcher

Per detected variant, it is shown whether this gene is already known to be associated to the HPO terms of that patient

  • “Lucid Genomics' cohort analysis tool has been a game changer for our research. It’s intuitive yet powerful, allowing us to quickly compare patient groups and uncover key insights. The platform has streamlined our workflow and enabled faster, data-driven decisions.”

    Felix Boschann -

    Medical Geneticist, Charité

  • “As a medical geneticist, Lucid Genome Suite has been a game-changer for analyzing and interpreting whole genome data. It provides comprehensive insights into coding and non-coding small, tandem and structural variants. It's intuitive, efficient, and has significantly streamlined the workflow.”

    Ehsan G. Karimiani MD, PhD -

    Medical Geneticist, UCL London

  • “Lucid Genomics' platform allows our team to quickly identify genetic variants and actionable insights with incredible precision. The intuitive interface and seamless cloud-based collaboration tools have transformed how we analyze and share large datasets across research teams.”

    Marco Savarese -

    Principal Investigator, Folkhalsan Research Center

  • “Lucid Genomics cracked 25-year-old unsolved cases — revealing hidden variants and redefining how we see the genome. Simply one of the the best tools to unlock the Dark Genome.”

    Prof. Pawel Stankiewicz, M.D., Ph.D. -

    Principal Investigator, Baylor College of Medicine

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