Lucid Genomics Webinar

​🚀 Join the Lucid Webinar: A Sneak Preview of the Future of Genomics - Integrating Whole Genome Analysis with Methylation Data

​Labs have invested heavily in long-read sequencing platforms - yet turning that data into actionable biological insight remains a major challenge. In this session, we'll give you an exclusive first look at where clinical genomics is heading.

​🧬 We'll preview the next generation of the Lucid Whole Genome Analysis Platform, built for intuitive, end-to-end analysis of long-read data — with methylation as a first-class layer, not an afterthought.

​✔️ Native integration of methylation data and Differentially Methylated Regions (DMRs) alongside sequence variants in a single analysis
✔️ Advanced detection and interpretation of structural variants and tandem repeats
✔️ Integrated multi-omics analysis (Hi-C, ChIP-seq, RNA-seq) to accelerate identification of causative pathogenic variants
✔️ Support for Adaptive Sampling, panel, and WGS data

​Whether you work in rare disease, complex traits, or translational research, you'll see how combining whole genome and methylation analysis unlocks insights that neither can deliver alone — and get an early look at features before they're released.

​Seats are limited. Reserve yours today.

​📅 October 13h

​🕓 4 PM CET | 10 AM EST

​💻 Online Webinar