ASHG 2026 · Tools, software & services

SeqOne at ASHG 2026

Wilmington, Delaware

SeqOne at ASHG 2026 in Montréal: 2 presentations (2 posters); Booth 521.

2
presentations on the program
1
Reviewers’ Choice abstracts
521
exhibit booth

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OrganizationASHG 2026 Attendance
SeqOne
Wilmington, Delaware
1 Data Science Engineer · 1 VP Product
Private company~125 people
SeqOne sells AI-powered NGS bioinformatics to molecular labs, helping them turn sequencing data into fast, actionable clinical insights.
SeqOne's Spring 2026 release added 72 IVDR-certified features, including structural-variant and lab-automation capabilities, a compliance-ready upgrade.
SeqOne's Spring 2026 release added 72 IVDR-certified features, including structural-variant and lab-automation capabilities, a compliance-ready upgrade.
2026-04 · source
SeqOne launched SomaLBx and SomaMethyl, two integrated solutions for in-house liquid-biopsy analysis in oncology.
2025-11 · source
SeqOne agreed to acquire Congenica, a UK company spun out of the Wellcome Sanger Institute, expanding its clinical genomics reach.
2025-09 · source
Source: company newsroom
Raised €20M growth round (May 2025)
Led by Supernova Invest with Elaia, Omnes, and Mérieux Equity Partners; oversubscribed round. · 2025-05-22
“SeqOne today announced a significant €20 million oversubscribed growth funding round. Led by new investor Supernova Invest”
Source: funding announcement
Currently hiring: 3 open roles
Source: careers page
Booth
Exhibiting at Booth 521
Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm
Poster
Wed Oct 21
2:30 pm
★ Reviewers’ Choice
Real-World Clinical Validation of DiagAI for WGS Interpretation in the NHS-GMS: Robust Prioritization and Rescue of Pseudogene-Masked Variants
Artificial Intelligence and Machine Learning
BioinformaticsCharacterization of disordersComplex diseasesExome/genome sequencing
Poster
Fri Oct 23
2:30 pm
Detection and Classification of Uniparental Disomy from Clinical Whole-Exome Data Using the GermVar Pipeline
Artificial Intelligence and Machine Learning
BioinformaticsClinical geneticsComplex diseasesCopy number/structural variation

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