Lucid Genomics

Lucid Genome Suite is an AI driven genomics interpretation platform that helps researchers and labs analyze whole genome or exome data across both coding and non coding regions, and across short read and long read technologies. It supports end to end secondary plus tertiary analysis to turn raw sequencing data into prioritized, interpretable variants.

What we can do:

• Ingest common genomics inputs (FASTQ, BAM, VCF) in a GDPR compliant, cloud hosted setup.

• Detect and interpret major variant types in one place, including SNVs, structural variants, and tandem repeats, across WES and WGS.

• Prioritize variants with AI based scoring and reduce false positives, especially in structural variant interpretation.

• Run cohort analysis for gene hunting and association style workflows, with phenotype and panel driven filtering.

• Support multi omics context (for example RNA seq and epigenetic layers), plus read level visualization and collaboration features for review and sharing.