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Diageno is your Next-Best-Step Diagnostic Copilot tool that utilizes patient HPO, phenotype, genotype, and declassified medical data to give informed next steps and potential diagnoses.
The Algorithm Finds It. The Community Decides It. A Compass for Rare Disease Research and Advocacy.
A companion diagnostic for complement-targeted trials. Model how biomarker-enriched patient selection reduces required enrollment and cost. Screen patients by complement activation profile.
Platform for Recurrent Respiratory Papillomatosis that matches similar patient profiles to aggregate real-world therapeutic outcomes and support evidence-guided care decisions.
Symtrack helps you easily log and track your symptoms, visualize patterns, and gain insights, empowering you to understand your health and take control of your well-being.
A shared timeline for rare disease. Our algorithm transforms daily logs into a color-coded map, allowing patients, doctors, and teachers to collaborate and turn reactive flares to proactive care.
Engineering Endpoints for Tiny Cohorts
PRANA is a patient companion for rare diseases that lets patients set their own life goals, tracks their symptoms.
OriGen resolves previously undiagnosed rare disease cases by interpreting genetic variants through protein structure and molecular mechanism, overcoming data scarcity and functional uncertainty.
A steady voice when the road feels uncertain
A clinician oriented copilot for help in rare genetic diseases diagnoses that allows clinicians to compare similar patients and recommends the best next steps in the diagnostic process.
Accuracy in every move
Prader-Willi Syndrome Vagus Nerve Stimulation and Monitoring
reviGen reanalyzes patient symptoms, family history, and genetic data to reduce diagnostic delays in unsolved cases, guiding clinicians to the right specialists with up to date genomic insights.
VIRTUOUS is a platform for VDM that lets patients recreate and share what they see through a visual emulator, generating structured records to improve clinical communication and awareness.
A structural diffusion framework for rare disease interpretation.
Don't get knocked out
JeevanSetu : Proactive Thalassemia care. We use Time-Series AI to predict blood needs & OCR/NLP for HLA matching. GenAI-driven retention transforms reactive crisis into predictive genetic precision.
Gene-ie transforms genes into treatment leads — using GNN intelligence and structured LLM reasoning to deliver transparent, safety-aware drug repurposing for rare diseases.
Multimodal Diagnostic Copilot for Rare Neurological Disorders
An automated prioritization engine that takes a patient's VUSs and ranks the variant most likely to be pathogenic, showing exactly where it sits in the protein's structure.
Protecting every breath while you sleep.
Digital health consultant and predictor—master your energy, predict your day, and validate the invisible.
CareConsole.ai — Your health baseline. Your early warning system.
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