Basel · 13 and 14 October We are at NextGen Omics, Tech & Data 2026, booth 20. Come and say hello. Basel NextGen Omics, 13 and 14 Oct, booth 20
Where Data Meets Intuition
Standardised, modular omics data analysis across your instruments, assays and kits. Built with your team, run in your own environment.
Keywords

Multi-omics analysis, Omics data analysis, Ready-to-run omics analysis, Raw sequencing data analysis, Reproducible bioinformatics, Bioinformatics on your own infrastructure, ISO 27001, Genomics, Transcriptomics, Proteomics, Metabolomics, Lipidomics, Single-cell, Spatial, Data Intuitive

Multi-omics analysis
your scientists run themselves.

Pharma-grade, tested omics analysis on your infrastructure.

We work with single research groups and with top-five pharma

  • From raw sequencing output to interpretation-ready results
  • One modular approach across instruments, assays and kits
  • Runs in your environment, your data never leaves
  • Every module tested and version-pinned, every run reported
  • Built with your bioinformaticians or ours

45 minutes, no slide deck.

Since 2018 in pharma production
300+ version-pinned modules, in production at two top-five pharma
ISO 27001 certified
Modalities
  • Genomics
  • Transcriptomics
  • Proteomics
  • Metabolomics
  • Lipidomics
Resolution
  • Bulk
  • Single-cell
  • Spatial
Janssen UZ Gent VIB Pfizer CZ Biohub Johnson & Johnson Cellarity Cytosurge Helmholtz GSK Virus Bank CZI
Our offering

How we work with you

Services

Our scientists run the analysis for you or work alongside your team. Either way, you receive the results together with the methods, quality checks and run report behind them.

See our services →

Catalogue

Tested, version-pinned analyses across instruments, assays and kits. If yours is not there yet, we build it as part of your project.

Delivery platform

The platform delivers the analysis to your own infrastructure. Your scientists pick it, set the parameters and run it themselves.

Watch the demo →
Interface beta programme

Help shape the interface against your own workflows

The next version of our delivery platform interface is being built now. The interface is where a scientist picks an analysis, sets the parameters, starts the run and reads the report, without writing code. A small group runs their own analyses on it and tells us what works and what gets in the way. What we ask for is your time and honest feedback on how the work really runs in your lab.

Limited seats · October 2026 to February 2027 · No cost for the programme

Who runs this

We can run thousands of samples without asking whether we trust the pipeline.

Single Cell Analysis Group Leader, global pharmaceutical company Source →

The same analysis runs for a small team and for pharma R&D.

Walk through a transcriptomics run end to end

Platform demo

A six-step wizard from experiment type to a ready-to-run analysis, the same path you would follow inside the platform. It ends in the outputs you get back: processed data, QC reports, results tables and figures.

This demo only covers a subset of transcriptomics analyses on Illumina, Element Biosciences and 10x. The full catalogue carries many more experiments, instruments and kits.

This is a web mockup of the application, not the application itself. Ask us for a demo of the real thing.

  1. 01 Modality
  2. 02 Kit / assay
  3. 03 Instrument
  4. 04 Experiment
  5. 05 Scenario
  6. 06 Review & run
Without the trade-off

Data and compute stay inside your security boundary.
Production-grade omics workflows run on top, fast and consistent.

Runs in your environment

Your sequencing data never leaves your environment. No uploads, no transfers, no waiting on data-transfer approvals. We deliver the analysis. Your data and compute stay with you.

Results you can stand behind

Same inputs, same workflow version, same answer, months or years later. When a reviewer asks you to regenerate a figure, you get exactly what you had before.

Fast, tested runs

Start your analysis the moment your run finishes. No waiting in the core-facility queue, no asking a bioinformatician to re-build the workflow for every project.

Regulated and clinical

Built for research. Documented for regulation.

Every run produces a quality report from the first experiment. If an assay later enters IVDR or GxP-regulated work, the record already exists.

We supply the platform and its qualification documentation. You own the validation.

In every quality report

  • How the analysis was executed
  • Which tools and versions were used
  • By whom
  • And when

Private deployments include a validation support package following

  • GAMP 5
  • 21 CFR Part 11
  • EU GMP Annex 11
See compliance services
Getting started

What you need to start

Your cloud account

You provide

  • An active AWS, Google Cloud or Azure account your team manages
  • Someone with admin access for the initial setup, usually from IT, platform or cloud-ops
  • A storage bucket the compute can read and write

We can provide for you

Do not have this yet? We can prepare the cloud storage setup for you. Infrastructure setup

On-premise

You provide

  • A Windows, Mac or Linux machine
  • Permission to install software on that machine
  • A current laptop is fine to start. Bigger datasets need a strong workstation in the lab

We can provide for you

Do not have this yet? We can prepare the on-premise setup for you.

Team

Scientists who build production software

We're computational biologists, bioinformaticians and software engineers, most of us PhD scientists. We understand your experiments and your data, and the messy reality of getting an assay from sample to result.

More about us
Data Intuitive bioinformatics team
The first step