All-in-one AI-powered platform for precise, scalable, and comprehensive genomic analysis

Unlock AI-driven insights for variant detection, prioritization, and interpretation at Individual, Family, and Cohort level in one solution.

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.

Integrated visualizations for hypothesis generation

Gain deeper insights into mutation effects with integrated visual tools.

  • Automated IGV-like visualizations of sequencing data across index patients, related and control individuals.

  • A clear regulome overview for streamlined analysis.

Prioritization for faster diagnosis

Using an advanced scoring system based on epigenetic data and our disease-agnostic AI model, we provide fast and reliable variant prioritization, accelerating the path to an accurate diagnosis.

Improved communication through Collab

Users can share and discuss findings using our Collab feature, thereby easily streamlining the collaboration between team members.

Technology-agnostic analysis

Supports all sequencing technologies, processing data and guiding you to accurate diagnoses, no matter your chosen path.

  • Short-reads

    e.g. Illumina

  • Long-reads

    e.g. PacBio

  • Linked-reads

    e.g TELL-Seq

  • Optical mapping

    e.g. Bionano

Genetic analysis across
data types

Analyzes data from panels to genomes, providing a manageable, prioritized list of suggested causative pathogenic mutations.

  • Whole genomes

  • Gene panels

  • Exomes

  • RNA-seq

  • Hi-C

  • ChIP-seq

Select the option tailored to your needs

Lucid CORE Lucid COHORT Lucid 360°
Data formats ✔ VCF ✔ FastQ or BAM ✔ FastQ or BAM
GDPR compliance ✔ Yes ✔ Yes ✔ Yes
Hosting service ✔ AWS ✔ AWS ✔ AWS, on-prem
Genome scope ✔ Coding & non-coding ✔ Coding & non-coding ✔ Coding & non-coding
Analysis level ✔ Individual & family ✔ Individual & family, Cohort ✔ Individual & family, Cohort
Technology scope ✔ Short- & long-reads ✔ Short- & long-reads ✔ Short- & long-reads
Technology integrative solution ✔ WES or WGS ✔ WES or WGS ✔ WES & WGS combined
AI prioritization ✔ Yes ✔ Yes ✔ Yes
Fast IGV-like visualization of aligned reads ✔ Yes ✔ Yes ✔ Yes
Collaboration/ Variant sharing ✔ Yes ✔ Yes ✔ Yes
Variant scope AI-Interpretation ✔ SV & Tandem repeat ✔ SNV, SV & Tandem repeat ✔ SNV, SV & Tandem repeat
Variant scope AI-Detection ✔ SNV & SV ✔ SNV & SV
Multi-omics integration ✔ RNA-seq & WGBS ✔ RNA-seq, WGBS, Epigenetics & Hi-C
Variant Enrichment / Burden Test ✔ Yes

End-to-End bioinformatic solutions

Simplify your workflow with a fully integrated pipeline: from Fastq to VCF to the interface platform.

  • FastQ

  • BAM

  • VCF

Used and trusted by leading experts

“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, 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, Kensington International Clinic

Discover our Platform

Get a personalized walkthrough of our platform and see how it can benefit your needs.