From Raw Data to Reliable Results. In Clicks, Not Code
Validated nf-core pipelines from raw sequencing data to reproducible insights. Automated for reliability, with Notebooks for deeper exploration.
Pan.bio is the AI-powered, end-to-end genomics platform connecting bioinformatics workflows, variant interpretation, and patient cohort data, all in one place. Built privacy-first with in-country deployment and HIPAA, GDPR, SOC 2, and ISO 27001 compliance baked into the architecture.
Trusted by scientists and researchers from
Platform
From raw sequencing data to clinical reports to cohort discovery, Pan.bio brings the entire genomic workflow into a single AI-powered platform; so teams stop stitching tools together and start delivering results.
Validated nf-core pipelines from raw sequencing data to reproducible insights. Automated for reliability, with Notebooks for deeper exploration.
A pre-configured notebook environment where BioMind generates code, debugs errors, and helps turn one-off discoveries into reusable team workflows.
Guideline-aware clinical variant classification powered by ACMG/AMP, CanVIG, ACGS, and ClinGen. AI-assisted, human-controlled.
Connecting hospitals and labs with pharma and biotech researchers. Unlock underrepresented populations while keeping data under provider ownership at every step.
Solutions
Five teams. One platform. Tailored to each.
Validated pipelines, AI-assisted notebooks, and shared workflows your whole team can standardize on.
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Guideline-aware classification grounded in ACMG/AMP, CanVIG, ACGS, and ClinGen with AI assistance for the hard cases.
Population-specific patient data from MENA and South Asia, assembled in weeks, not months.
Monetize de-identified clinical data without losing ownership, jurisdiction, or compliance.
Reproducible pipelines, multi-tenant isolation, and a unified AI layer to scale your operations.
Our Reach
Trusted by scientists from leading research labs, hospitals, and clinical institutions worldwide.
Why Pan.bio
Everything an advanced genomics operation needs, privacy, access, and intelligence, in one platform.
Deploy on your country’s compliant cloud or on-premise. Data never leaves your jurisdiction.
Population-specific cohorts and references for MENA and South Asia, populations missing from every major public database.
Run validated pipelines through a clean interface, or describe what you need to BioMind in plain English.
Sequencing → pipelines → variant interpretation → clinical reports → cohort discovery, all in one platform.
BioMind is a unified AI copilot that adapts to every product, not three separate bots bolted on.
HIPAA, GDPR, SOC 2 Type 2, and ISO 27001 enforced at the infrastructure level, not as documentation your team manages.
About Pan.bio
Pan.bio exists to empower scientists to transform genomic data into scientific breakthroughs. We build the AI-powered, end-to-end platform that bridges the distance between raw sequences and world-changing insights, making genomic research faster, more accurate, and accessible to teams who've been left out of the global research conversation for too long.
Our focus on underrepresented populations isn't a marketing line, it's the reason we exist. From MENA breast cancer research to Pan-Arab diabetes cohorts, we're building the infrastructure that lets clinicians, researchers, and pharma teams generate the genomic insights their populations have been missing from for decades.
"We're not just building software, we're building equity in genomics."
Enforced at the infrastructure level, your data stays in your jurisdiction, always.
researchers trust Pan.bio to power their genomic discovery
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