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AI-powered NGS Diagnostics
& Genomics Research Platform
About Impactomics
Life sciences and healthcare teams process unprecedented volumes of genomic, clinical, and real-world data. Yet fragmented tooling, regulatory friction, and legacy infrastructure slow the path from signal to validated action.
ClairLabs brings you Impactomics – integrating multi-omics NGS, bioinformatics, agentic AI, and cloud engineering with enterprise data governance. Transform raw NGS data into actionable clinical insights for rare diseases, oncology, and precision medicine. Accelerate scientific outcomes through FASTQ, audit-ready reports, and more to bridge the gap between sequencing and clinical decision-making – with the speed, accuracy, and compliance rigor for modern health and diagnostics demand.
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The Impact We Make
Pathogenic variant
ranking accuracy
Reduction in manual
curation burden
Patient samples
validated
Compliant
Infrastructure
Our Transformative Offerings
& Cloud Migration
Modernize legacy bioinformatics: automated QC, variant calling, annotation, and audit-ready reporting—cloud-native, reproducible pipelines that scale diagnostics from pilot to production.
Data Lakes & Integration
Secure, governed genomic data lakes with FHIR/HL7/OMOP and GA4GH interoperability; federated learning and role-based access for compliant, auditable AI collaboration.
AI-powered variant ranking, AutoACMG classification, and multi-omics evidence integration—deliver clinician-ready, explainable reports that cut time-to-diagnosis and reduce analyst burden.
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& Biomarker Prioritization
RAG-enabled literature mining and dynamic prioritization pipelines to accelerate target discovery, companion diagnostic design, and translational validation.
Introducing VarMiner Cloud
Your one-stop solution to derive maximum value from your genomics data
Drive a future-proof precision medicine pipeline powered by cloud-enabled genomics architecture, precision medicine platform design, and scalable bioinformatics for compliant, production-grade operations.
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How Impactomics Empowers You
Agentic AI ranks variants, applies ACMG rules, and creates explainable evidence maps for rapid review and insightful next-steps.
Outcome: Faster reports, higher productivity, consistency, and lower costs.
LLMs extract HPO terms, ontology-match them to OMIM/Orphanet, and rank genes by phenotype and evidence to identify explainable candidate diagnoses.
Outcome: Faster diagnosis, higher yield.
Agentic orchestration inspects BAM/VCF metrics, flags anomalies, triggers re-runs or review, and logs decisions for audit readiness.
Outcome: Faster QC, fewer errors, audit-ready records.
RAG agents mine knowledge bases and literature to prioritize druggable targets, score candidates by biology and clinical evidence, propose validation paths.
Outcome: Faster validation, de-risked R&D.
GenAI correlates transcriptomics, methylation, proteomics, and variants to propose ranked biomarker panels and validation plans
Outcome: Novel biomarker insights, faster translational validation.
Index FASTQ/BAM/VCF with clinical metadata, create model-ready cohorts, enable natural-language queries and packaged datasets for ML training.
Outcome:Faster AI training, democratized data insights.
How You Benefit
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Actionable AI for Multi-omics
Multi-omics
Produce clinician-ready insights and accelerate biomarker discovery within hours.
Scale NGS Pipelines to the Cloud
Process exponentially more samples with lower OPEX and faster TAT.
Single-source Data Fabric
Data Fabric
Harmonize LIMS, EHR, and research data into a governed, queryable lake.
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Compliance-first Managed Services
Managed Services HIPAA/GDPR, RBAC, audit trails, and 24/7 cloud operations you can trust.
What if you could turn your raw data into renewable revenue?
Monetize FASTQ-to-insight pipelines: sell validated biomarker panels, data subscriptions, and co-development deals for a sustainable and elevated bottom line.
Dive Into Our Capabilities
Integrate genomics, transcriptomics, proteomics, and epigenomics into harmonized datasets enabling cross-modal biomarker discovery and translational insights.
Validated pipelines and expert analysis for clinical-grade variant calling, annotation, and report generation with audit-ready traceability.
Clinical-grade AI models for variant interpretation, phenotype matching, and predictive analytics that improve diagnostic yield and speed decisions.
Managed model development, deployment, and monitoring with federated learning and governance to scale secure AI across institutions.
Partner with us to deploy Impactomics and unlock the full potential of your multi-omics data.