Comprehensive genome analysis at scale
Unlock insights with advanced AI-driven solutions for precise, scalable, and comprehensive genomic analysis.
Analysis of 100% DNA
The mutations in both coding and non-coding regions of the DNA are analyzed and scored based on their potential pathogenicity for comprehensive insights.
This ensures all the information acquired through DNA sequencing is fully extracted.
Fast large-scale cohort analysis
Analyze thousands of genes across hundreds of samples in just seconds, streamlining the process of identifying causative pathogenic mutations.
This speed enables quick diagnostics, delivering results efficiently without compromising accuracy or scalability.
Reducing false positives by 87%
Filter noisy datasets from short-read sequencing to filter out false positives and improve variant detection in complex regions.
This ensures all the information acquired through DNA sequencing is fully utilized.
All variants coverage
Detect the entire spectrum of mutations including SNVs, InDels, Repeat Expansions, and SVs.
This ensures full coverage of all variants, capturing critical information from the sequencing data.
Full multi-omics integration
Integrate a multi-layer analysis that combines epigenetic modifications, gene expression, and 3D genome interactions.
This comprehensive approach supports the prioritization and identification of mutations in genomes, offering deeper insights into genetic variations.
The ones trust us saying
“Lucid Genomics' platform integrates AI-driven algorithms allowing 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 Saverese - Principal Investigator, Folkhalsan Research Center
“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, Charite
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