Auracle Therapeutics

01 — Auracle™ Discovery Platform

Novel therapeutic targets, directly from patient data

Auracle is a deep learning platform that discovers novel drug targets directly from patient transcriptomics, ranking candidates by disease biology, not by prior druggability or target precedent.

02 — The Problem

Most target discovery platforms recycle what's already known

When computational models are trained on features like druggability scores and tractability indexes, they learn to predict what has already been targeted, sometimes missing what matters biologically. The output reflects the literature, not the disease.

Auracle removes that circularity entirely. Candidates are ranked by their position in patient-derived disease networks, scored by the biology. The result: targets that conventional approaches structurally miss.

03 — How It Works

We use patient transcriptomics to rank therapeutic hypotheses

Auracle builds patient-specific disease networks from transcriptomic data, then applies proprietary deep learning to score every gene by its topological importance instead of whether it has ever been drugged before.

01

Input

Patient Data

Gene expression from case-control cohorts. No proprietary formats required.

02

Model

Disease Networks

Patient-derived molecular interaction networks encoding disease-specific topology.

03

Engine

Auracle™PATENT PENDING

Proprietary deep learning trained on topology with built-in mechanistic interpretability.

04

Output

Ranked Candidates

Probability-scored therapeutic hypotheses with per-target mechanistic explanations.

04 — What Makes It Different

Built to find what hasn't been found

No druggability bias

Druggability and tractability scores are excluded from features and ranking. Candidates are scored by disease biology, not by what's convenient to target.

Cross-cohort generalization

Trained on one patient population, validated on completely independent cohorts without retraining. The model learns disease topology, not dataset artifacts.

Mechanistic interpretability

Every candidate comes with attention-derived explanations of which network interactions drove its ranking, not a black box.

05 — Validation

Tested blind against clinically validated targets

Held-out clinical targets the model never saw during training, evaluated against over 14,000 background genes across 201 patients from two independent cohorts.

0.97

Hold-out AUROC

201

Patients · 2 cohorts

14.8K

Background genes

Target Recovery — Blind Hold-Out Evaluation18 held-out clinical targets vs 14,819 background genes0.00.20.40.60.81.0Clinical targets recovered22.2%Top 5038.9%Top 10077.8%Top 500Genes ranked by model score

Blind evaluation on held-out clinical targets vs. 14,819 background genes. Rankings are driven by disease network topology, not simple connectivity (degree correlation r = 0.056).

Key findings replicated in a fully independent patient cohort (n = 161) with no shared data, no shared graph, and no retraining.

06 — Work With Us

You have the data. We'll find the targets.

We partner with pharma, biotech, and research teams who have transcriptomic data and want therapeutic hypotheses that haven't been generated before.

Pilot engagements start with a single disease cohort. We deliver ranked candidates with mechanistic explanations in weeks, not months.