Genomic Intelligence,
Simplified.
Smart bioinformatics pipelines transforming sequencing data into actionable insights.
Spend time on the What, not the How.
Our purpose-built bioinformatics pipelines handle the how, so your team can spend its time on the answers — not on getting there.
- UploadYour data, securely.
- AnalyseAutomated, standardised pipelines.
- InterpretActionable insights that matter.
How it works
How raw NGS data become insights?
Our purpose-led, focus-driven pipelines convert raw NGS into Answers! Everything happens in the background, allowing you to focus on the answers.
Featured product
Species ID for MTB/NTM and Drug Resistance report by analysing Raw NGS data to actionable clinical insights.
Explore Clariseq TB
Why Clariseq?
Multi-database consensus
Every variant is checked across public and curated resistance databases side by side, showing where evidence agrees — and where it differs.
Evidence you can trace
Every interpretation links back to its supporting database, publication, or scientific evidence. No unexplained black-box conclusions.
Insights that support clinical testing
Complex genomic data is translated into clear, clinically relevant insights, saving hours of complex work to enhance clinical decision making.
Security
Security, built into every layer.
Data security by design
Data is encrypted in transit and hosted on secured cloud infrastructure, with controlled access to genomic and account data.
Built around India’s DPDP Act
Privacy by design: responsible data-handling practices, with clear controls over how data is processed and retained.
Secure access & accountability
Role-based permissions and authenticated access safeguard sensitive workflows. Each account’s data stays separate, and administrator actions are logged.
Your data stays in India
Samples are uploaded, processed and stored on infrastructure located in India. Genomic data does not leave the country.