Multi-omics Intelligence & Management Solutions
Scale discovery with trusted AI and precision intelligence, engineered for impactful outcomes.
A Bird’s Eye View
Healthcare and life sciences leaders face fragmented datasets, scaling constraints, and stringent regulatory requirements that slow discovery. ClairLabs unifies multi-omics, including genomics, transcriptomics, proteomics, real-world clinical, and operational data on a cloud-native, AI-first platform, automating ingest, QC, integration, and explainable analytics.
We convert complexity into actionable biomarkers, reproducible pipelines, AI/ML- driven interpretation, and compliant reports. With these initiatives, we help pharma, diagnostics, and biotech accelerate trial-ready multi-omics support for translational research and clinical trials. Partner with us to shorten discovery timelines and scale clinical impact.
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
We enable clinical labs to integrate DNA, RNA, and other omics. Detect SNVs, indels, CNVs, fusions, and expression outliers, while delivering sensitive, specific companion diagnostics and interactive clinical dashboards.
We help design discovery platforms combining WGS/WES, RNA-Seq, epigenetics, and single-cell data to identify novel biomarker signatures, profile patients, and perform robust clinical validation across multi-site studies.
Fuse genomic, transcriptomic, proteomic, and metabolomic layers with clinical metadata using tailored AI/ML pipelines to reveal cross-omics mechanisms, patient stratification, and scalable, high-throughput biomarker discovery.
We leverage advanced analytics and agentic AI to harmonize heterogeneous datasets, automate cohort building across studies, and accelerate translational hypotheses with reproducible, explainable models for downstream trials.
We provide GxP-ready, secure data hosting and FAIR repositories with encrypted workspaces, provenance, and custom GenAI SLAs—enabling retrospective cohort mining, consortia collaboration, and regulatory audit readiness.
We help teams integrate scRNA-seq and ATAC-seq with spatial omics visualizations to map cellular states and microenvironments, enabling high-resolution biomarker localization, mechanistic insights, and discovery for translational studies.
How You Benefit
Faster Decisions
Harmonize multi-omics and clinical data to accelerate go/no-go decisions with confidence.Scalable Labs
Automate NGS workflows to increase throughput, reduce errors, and ensure compliance.Secure Governance
Centralize governed data with encryption, audit trails, and role controls.Actionable AI
Deploy explainable models that prioritize biomarkers, cohorts, and therapeutic targets.
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
Read more to obtain deep-cut insights on how to leverage multi-omics datasets to accelerate discovery.
Ready to transform your multi-omics data into clinical impact?