Products

NEBULA Respiratory Multi-Omics Database

Transforming respiratory biology into intelligence for drug discovery.

Close-up microscopic view of microbes in greenish tint.
WHat it is

The dataset respiratory discovery has been missing

NEBULA is Diag‑Nose’s in‑development nasal multi‑omics database, built to power respiratory biomarker discovery and drug development.

Helps research and pharma partners discover and validate novel biomarkers, identify disease subtypes, and understand disease and treatment-response biology by linking longitudinal nasal biomarker data to clinical outcomes.

Every dataset is collected using ABEL, our standardised nasal sampling method, so data stays comparable across studies and sites.

Supports partners to evaluate and de-risk pharmaceutical assets, train and validate biological models, and design smarter clinical trials and patient stratification strategies - generating new diagnostic and therapeutic hypotheses along the way.

NEBULA grows with every patient enrolled, building breadth and depth across respiratory indications over time.

Nebula stylized image with a cursor hovering over an empty, spreadsheet grid to represent respiratory database.
What NEBULA aims to do

From data to discovery

Identify novel targets

NEBULA aims to reveal molecular patterns associated with disease progression and therapeutic response, providing researchers with new starting points for target discovery.

Optimise candidate selection

By linking biomarker data to clinical outcomes, NEBULA aims to help pharma partners prioritise candidates for further investigation using biologically informed evidence.

Power validation & hypotheses

Built on longitudinal, clinically-linked data collected through a single standardised method, NEBULA gives pharma, biotech and research partners a foundation that grows more powerful with every study, enabling biomarker validation, hypothesis testing, and analytical models that fragmented or multi-source datasets simply cannot support.

Whats inside

Curated, longitudinal, clinically linked

Data · From company overview

  • Curated, longitudinal nasal multi-omics data
  • Linked to clinical metadata and treatment history
  • Organised by study and indication
  • Built on standardised ABEL collection
  • Grows cumulatively with every enrolled patient
Access

Secure, privacy-governed access

Partners access NEBULA through secure, privacy‑governed agreements.

The platform is being built to the compliance and governance standards that pharmaceutical and institutional research partnerships require.

Includes access controls, audit trails, and partner confidentiality protections, ensuring one partner’s queries and insights remain their own.

Designed to scale with partner needs, providing a discovery resource no single organisation could build independently.

availability

Pilot to launch

Data · Roadmap

01

In progress

Phase 01

Pilot access

Early access for partners.

2026

02

Planned

Phase 02

Launch

General availability.

2027

Conditions covered

Respiratory conditions in the dataset

Asthma

Chronic rhinosinusitis

COPD

Rhinitis

Infectious airway disease

Non-infectious lung disease

Focus Conditions

Common questions

Common questions

What is NEBULA?

An in-development, curated nasal multi-omics database for respiratory disease.

What does it contain?

Longitudinal nasal multi-omics data linked to clinical metadata and treatment history, organised by study and indication, built on standardised ABEL collection.

What does NEBULA aim to enable?

Target discovery, biomarker validation, hypothesis generation, and optimised drug candidate selection.

How do partners access it?

Through secure, privacy-governed agreements. Access method is confirmed at the partner stage.

Who is NEBULA for?

Biotech companies, researchers and pharmaceutical firms.

When is it available?

In development — pilot access 2026, launch 2027.

Nebula is an investigational technology. It has not been approved by the FDA or any other regulatory authority for diagnostic or clinical use.

RhinoMAP is an investigational technology. It has not been approved by the FDA or any other regulatory authority for diagnostic or clinical use.

RhinoMAP is an investigational technology. It has not been approved by the FDA or any other regulatory authority for diagnostic or clinical use.