Where AI in Genomics
Meets Clinical Impact
Meet Us At #Booth 1822
ASHG 2026 | October 20–24 | Montréal, Canada
Still grappling with genomics challenges? Leverage the new-age AI to solve them faster. See how precision diagnostics teams use AI to interpret variants, integrate multi-omics data, and scale clinical workflows without scaling headcount.
As variant interpretation bottlenecks and multi-omics integration become urgent, see how ClairLabs delivers AI-powered genomics workflows built for audit-ready clinical insight.
Impactomics
Our Flagship Multi-omics Platform
See how Impactomics powers end-to-end genomic data analysis, from raw FASTQ to clinical-grade reports. Built for clinical genomics laboratories and research teams that need speed, traceability, and compliance in a single platform.
What you'll see:
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• Automated NGS variant interpretation with ACMG-aligned classification |
• Phenotype-driven gene ranking that cuts analyst review time by half |
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• Real-time multi-omics correlation across genomic, transcriptomic, and more. |
• Scalable cloud genomics analysis pipelines with full audit trails |
ClairOS
Multi-agent AI for Variant Intelligence
ClairOS is an orchestrated, multi-agent AI system built for genomic data interpretation with AI. It coordinates specialized agents across variant calling, evidence synthesis, and classification — delivering faster, more consistent results than single-model approaches.
What you'll see:
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• Explainable AI that traces every classification back to its source evidence |
• Human-in-the-loop review workflows designed for clinical decision support (CDS) |
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• Compliance-ready architecture aligned with HIPAA, CLIA, and CAP standards |
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Meet Our Leaders at Booth #1822
Encountering business challenges that are costing
you time, accuracy, and throughput?
Our Focus Areas at ASHG 2026
This year's ASHG program reflects the exact challenges ClairLabs solves.Here's where our work intersects with the conference's most-watched themes.
ASHG 2026 hosts a dedicated workshop on best practices for AI in clinical genome analysis. ClairLabs has operationalized this. Our AI clinical decision support workflows deliver automated ACMG classification with explainable, traceable outputs.
A confirmed hands-on ASHG workshop focuses on using AI-enhanced multi-omics tools to solve rare and undiagnosed diseases. Impactomics integrates genome, exome, RNA-seq, and methylation data into one analytical layer.
As sequencing volumes outpace legacy systems, ClairLabs' cloud-native architecture and API-first data engineering let labs scale interpretation and reporting without scaling headcount, infrastructure spend, or specialist hiring.
ASHG's ELSI sessions address AI ethics, genetic privacy, and transparency. ClairLabs designs every solution with explainable AI at the core. No black boxes. Every recommendation is auditable.
From Our Thought Leaders’ Desk
Download our latest thought leadership content
How leading clinical genomics labs are using automation and AI to cut curation time while maintaining compliance.
A deep dive into what happens after sequencing, and how AI-powered genomics is closing the gap between raw data and clinical action.
An expert analysis of the five themes that will dominate this year's agenda, from AI in variant interpretation to globally representative genomics.
Related Solutions
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Deploy containerized NGS workflows on cloud-native infrastructure. Automate variant calling, annotation, and reporting for high-throughput genomic diagnostics and research.
Deploy containerized NGS workflows on cloud-native infrastructure. Automate variant calling, annotation, and reporting for high-throughput genomic diagnostics and research.
Deploy containerized NGS workflows on cloud-native infrastructure. Automate variant calling, annotation, and reporting for high-throughput genomic diagnostics and research.