
AI/Gen AI Solutions
Catalyzing growth and powering breakthroughs through AI-led intelligence
Life sciences and healthcare teams are faced with unprecedented volumes of genomic, clinical, and real-world data. However, fragmented tooling, regulatory friction, and legacy infrastructure slow the path from signal to validated action.
At ClairLabs, we bridge science and scale, combining multi-omics, NGS, bioinformatics, agentic AI, and cloud engineering with enterprise data governance to convert raw omics into auditable, decision-ready intelligence.
Transformative Consulting Offerings

We design and optimize end to end NGS pipelines, automating QC, variant calling, annotation and regulatory grade reporting. Harmonize multi-omics data and migrate bioinformatics to cloud-native platforms for reproducible diagnostics.

We build HIPAA and GDPR compliant data lakes, that enable firms to migrate their legacy systems to cloud microservices, implement FHIR, HL7, OMOP and GA4GH interoperability. Enable federated learning to train secure cross institutional AI.

We advise labs on LIMS and ELN modernization. We also design API first microservices to replace monoliths, craft clinician friendly UX, dashboards, and AI copilots that streamline workflows and accelerate decision making.

We design infrastructure and workflows meeting HIPAA, GDPR, CLIA and CAP. Implement auditability, logging, governance; apply threat modeling, encryption and secure APIs to protect patient genomics and clinical data at scale.

We implement AI diagnostic systems for variant interpretation, risk stratification, and predictive modeling. Integrate Gen AI for literature synthesis and matching. Leverage agentic workflows and digital twins to personalize and accelerate decisions.
How ClairLabs Empowers You
Deploy Agentic AI to parse VCFs, integrate ClinVar/COSMIC/OMIM, apply ACMG/AMP rules, and drafts explainable clinical interpretations. Cut down manual curation by 70–80%, improving consistency, auditability and diagnostic turnaround time.
Utilize LLM agents to map HPO terms from clinical notes to OMIM/Orphanet/ClinGen associations using ontology reasoning, producing evidence-based gene rankings that speed rare-disease diagnosis and reduce time-to-result.
Leverage agentic orchestration to inspect BAM/VCF QC metrics. Get accurate reports on depth, VAF, strand bias, and auto-flag anomalies before reporting, to ensure analytical validity, reduce manual QC burden, and downstream rework for compliant, audit-ready pipelines.
Use RAG-powered agents mine TCGA/GTEx/GEO and literature to rank disease-relevant, druggable targets. Drive dynamic, data-backed target maps and prioritizing candidates for rapid validation, cutting early discovery timelines by >50%.
Utilize Gen AI to interpret multi-omics correlations across RNA-seq, methylation and proteomics to propose biomarker–disease–drug hypotheses, accelerate translational validation, and establish companion-diagnostic development and commercialization readiness.
Effortlessly index and monitor cloud-native genomics data lakes (FASTQ/BAM/VCF), enable natural-language “ask your data” queries with Gen AI agents, and provision model-ready annotations to accelerate AI training and discovery workflows.
How You Benefit
Scale & deliver NGS pipelines to the cloud :
Drive faster turnaround, lower OPEX, and auditable reportingActionable AI for multi-omics
Prioritize variants, auto-generate clinical summaries, and speed biomarker/target discoverySingle-source data fabric
Harmonize multi-omics, HER, and registry data into governed lakes for reproducible analyticsCompliance-first managed services
HIPAA/GDPR-ready controls, role-based access, audit trails, and 24×7 cloud operations

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.
.jpg?width=300&name=048fe5e71d05e92b27c3f32758269d2404fe5aff%20(1).jpg)
Deploy containerized NGS workflows on cloud-native infrastructure. Automate variant calling, annotation, and reporting for high-throughput genomic diagnostics and research.
.jpg?width=300&name=048fe5e71d05e92b27c3f32758269d2404fe5aff%20(1).jpg)
Deploy containerized NGS workflows on cloud-native infrastructure. Automate variant calling, annotation, and reporting for high-throughput genomic diagnostics and research.
Dive Into Our Capabilities
Uncover Insights
Description: Read more to obtain deep-cut insights on how to go from raw data to decision-ready intelligence
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Partner with ClairLabs to deploy Gen AI & Agentic AI solutions that drive innovation, compliance, and measurable outcomes.