Lucid Genomics at ASHG 2026

Oct 20–24, 2026 Montréal, Canada ~7.5k attendees Website

Lucid Genomics brings 1 presentation to ASHG 2026 in Montréal, and exhibits at Booth 307. Its program centres on long-read genomic data analysis, rare-disease cases, and variant interpretation. It presents LGS for testing and evaluating variant interpretation and detection software.

OrganizationASHG 2026 Attendance
Lucid Genomics
Berlin, Germany
1 CEO and Managing Director
Private company
Lucid sells cloud-native software for secondary and tertiary analysis of long-read genomic data. It serves clinical laboratories, research institutions, and biotechnology companies.
Partnered with Genetic Alliance to give in-kind access to its AI-native genomic analysis platform for rare-disease cases.
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Partnered with Genetic Alliance to give in-kind access to its AI-native genomic analysis platform for rare-disease cases.
2026-07 · source
Had its tertiary analysis pipeline validated by Oxford Nanopore, confirming it works with Nanopore sequencing data.
2026-05 · source
Partnered with QIAGEN to give its customers a path to long-read interpretation, widening Lucid's distribution reach.
2026-04 · source
Source: company newsroom
€1.3M pre-seed round led by Caesar Ventures (Sep 2024)
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A small early-stage round, not recent revenue; other backers included BIF Partners and Another.Vc. · 2024-09-02
“raised €1.3 million pre-seed funding round led by Caesar Ventures, with additional support from BIF Partners, Another.Vc, and the MPF Accelerator Program.”
Source: funding announcement
No openings posted
Booth
Exhibiting at Booth 307
Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm
Poster
Wed Oct 21
2:30 pm
LGS: testing and evaluating a novel variant interpretation and detection software
Collaborators: Max Planck Institute for Molecular Genetics, MSB Medical School Berlin +1 more
Bone/joint abnormalitiesMalformationArtificial intelligenceSkeletal system

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