Glioma Spina Bifida Tethered Cord Hydrocephalus Dandy-Walker Encephalocele Arachnoid Cysts Craniosynostosis Chiari Malformation
01 / 09 Live AURORA-GLIO

Glioma

Gliomata

End-to-end stack for the most lethal primary brain tumor.

Glioblastoma and lower-grade gliomas remain the deadliest primary brain cancers. AURORA-GLIO unifies molecular profiling, radiomics, surgical planning, ethics and clinical translation into a single auditable, open pipeline.

Subsystems 11
Scope Adult & paediatric · WHO 2021 aligned
Readiness Spec frozen · prototypes building
Pilots 3 pilot sites scoping
Latency target target <150ms
License MIT

The clinical problem

Glioma is the most common malignant primary brain tumor in adults. Median survival in glioblastoma sits around 15 months despite four decades of trials. Heterogeneity — across patients and inside a single tumor — is the central problem AURORA-GLIO is built to address.

Built with and for
Neuro-oncology surgeons Radiologists Computational biologists Trialists

Platform demo

What a node running AURORA-GLIO is designed to do, from connecting a source to signing off on what may leave the building. Six steps, drawing on the module's 11 specified subsystems at step three.

The console below is a design mock, not a screenshot of running software. Status pills such as “connected” and “running” depict intended states, and every identifier, count and score is fabricated for demonstration — no patient data, no measured performance, no clinical output. What the sequence is meant to show is where the human sits and what the boundary permits.

aurora-node · demo-site.internal egress: aggregates only

Connect the sources you already have

step 1 of 6

The node reads your PACS and FHIR endpoint from inside your network. Nothing is copied out, and no inbound path to patient data is opened from outside.

Source adapters · demo-site.internal
DICOM C-FIND / C-MOVE connected
FHIR R4 — Patient, Condition, ImagingStudy connected
Outbound path to AURORA none
Module enabled AURORA-GLIO
boundary

Adapters run inside the perimeter. At this point the node can read records and cannot send anything anywhere.

Recorded walkthrough

Drop a screen recording still or poster frame here. No recording exists yet — this is a slot, not a hidden video.

What a real demo requires
  • Ethics or IRB approval covering the cohort being shown.
  • A site willing to be named, or a fully synthetic dataset built for the recording.
  • Clinician review of every frame that shows an output.
  • A version pin, so the recording matches the code it depicts.
Request a live walkthrough →

Subsystems

Live 7 Beta 3 Soon 1

11 subsystems, each a vertical slice with its own specification. The states below track build progress against that spec — they are not evaluation results and not regulatory status. Module readiness overall: “Spec frozen · prototypes building”.

  • 01 Systems Atlas GLIO-SYS Multi-omic systems map of glial lineages, niches and signalling. Live
  • 02 Macro-Micro Bridge GLIO-MMB Connects scanner-scale imaging with cell-scale histology features. Live
  • 03 Tumor Microenvironment GLIO-TME Immune-stromal-vascular crosstalk simulator with spatial priors. Live
  • 04 Foundation Models GLIO-AI Pre-trained vision-language-omics transformer for glioma. Live
  • 05 Infiltration Field GLIO-INFIL Diffusion-reaction PDE solver for invasive margins beyond contrast. Live
  • 06 Causal Trajectories GLIO-CAUS Counterfactual graphs over treatment, resection and progression. Beta
  • 07 Integrated Diagnosis GLIO-DIAG WHO-aligned molecular + histo + radio diagnostic synthesizer. Live
  • 08 Radiotherapy Plan GLIO-RAD Auto-contoured GTV/CTV/PTV with dose-response priors. Beta
  • 09 Clinical Trials GLIO-CLIN Eligibility matcher and adaptive arm allocator for active studies. Beta
  • 10 Ethics & Governance GLIO-ETHIC Bias, consent and equity audit layer with provenance reports. Live
  • 11 Organoid Twin GLIO-ORG Patient-derived organoid digital twin synced with bench data. Soon

For patients and families

The same condition, written for the people living with it: 50 plain-language guides and 265 defined terms, with no methodology and no jargon left unexplained.

Evidence & oversight

Every module must move through the same four gates before any clinical use, and each gate can send it back rather than forward.

No AURORA module has entered this pathway. Every gate below reads not started, and will continue to until a real result is published and the site that produced it has agreed to be named. Build progress on the subsystems above is not evidence of clinical validity.

1 Retrospective validation Not started Held-out data from sites that took no part in development.
2 Silent prospective Not started Runs alongside standard care with no output shown to clinicians.
3 Supervised clinical evaluation Not started Prospective, under ethics approval, reported to DECIDE-AI.
4 Post-market monitoring Not started Continuous performance and drift tracking; degradation withdraws the module.
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