How GenoBank.io™ Transforms Genomic Data into Programmable AI Training Assets Through BioIP Protocol
The Problem: 547 million genomic datasets worth $97.5 billion sit locked in corporate silos, inaccessible for AI training.
The Solution: GenoBank.io™ transforms genomic data into programmable BioNFT™ assets on Story Protocol, enabling patient ownership and AI licensing.
The Opportunity: Create the first patient-owned AI training marketplace where data owners earn 15% of all commercial use, starting with 780 live datasets and scaling to 25K by 2027.
Note: All valuations based on EY Report: How we can place a value on health care data
Data Holder | Market Value | AI Training Assets | Asset Type | Patient Access |
---|---|---|---|---|
IQVIA Holdings | $33.8B (£26.0B) | 530M patient records | Clinical + Genomic | No API/No Access |
Illumina | $44.1B (£33.9B) | Millions sequenced | Raw Sequence Data | No API/No Access |
23andMe | $2.6B (£2.0B) | 15M genomes | Consumer Genomics | Download Only |
Exact Sciences | $7.4B (£5.7B) | ~2M samples | Cancer Genomics | No API/No Access |
Foundation Medicine | $2.5B (£1.9B) | 400K profiles | Tumor Genomics | No API/No Access |
Grail | $7.4B (£5.7B) | 140K NHS samples | Early Detection | No API/No Access |
Total Locked Assets | $97.8B (£75.2B) | 547.5M+ Records | Prime AI Training Data | 0% Accessible |
Key Insight: These 547M datasets represent the ultimate frontier for healthcare AI, yet remain completely inaccessible for training drug discovery models, disease prediction algorithms, and personalized medicine AI.
AI Training Data Type | Current Market Rate | Quality Score | Availability |
---|---|---|---|
Text Data (Web Scrapes) | $0.01-0.10 per MB | Low-Medium | Abundant |
Image Datasets | $0.50-5.00 per image | Medium | Common |
Medical Imaging | $10-100 per scan | High | Limited |
Genomic Data (Current) | Not Available | Highest | Corporate Silos |
BioNFT™ Genomic Data (2027) | $100-500 per genome/year | Highest + Verified | Story Protocol |
EY Report Finding: Foundation Medicine and Flatiron were acquired by Roche yielding an estimate of US$6,000 per genomic record and US$950 per clinical record, demonstrating how combining genomic data with patient histories creates a 6x value multiplier.
The SomosDAO collection demonstrates how genomic data becomes programmable AI training assets. These 780 real 23andMe genotype datasets are already generating value through Story Protocol's infrastructure:
780 23andMe Genotype Datasets
View the complete collection on Story Protocol Explorer:
Explore Collection on Story →EY Report Finding: "Having genetic information and longitudinal data allows us to paint the clearest picture on patient epidemiology, progression, and overall experience." - Director, Field Health Outcomes, Pharmaceutical company
Data Maturity Stage | Description | EY Benchmark Value (USD) | Enhancement Factor |
---|---|---|---|
Raw Data | Basic sequencing, ancestry data | $125 | 1x baseline |
Curated | Organized, validated, quality-checked | $625 | 5x enhancement |
Longitudinal | Aggregated over time with clinical history | $1,250 | 10x enhancement |
Analyzed | With insights, predictions, and annotations | $6,250 | 50x enhancement |
Actionable | Clinical-grade, treatment-informing data | $12,500+ | 100x+ enhancement |
Data Type | EY Benchmark Value (USD) | Example Transactions |
---|---|---|
Raw 23andMe genotype data | $20 (ancestry only) | Consumer direct-to-consumer baseline |
EHR/EMR data | >$125 per record | Electronic health records |
Genomic data aggregators | >$1,875 per DNA sample | Private equity valuations |
Genomic + phenotypic combined | $1,250-$6,250 per record | Foundation Medicine: $7,500/record |
23andMe + GSK collaboration | $493 per record | 5M records, $2.46B valuation |
Value Enhancement Strategy: Starting with 780 23andMe genotype datasets ($20 baseline value each), GenoBank's BioIP™ protocol enables progression toward EY-benchmarked values of $1,250-2,500 per enhanced dataset through clinical integration and patient ownership models.
While Grail built a $7.1B company using centralized patient data, we're building Grail 3.0 where patients own their genomic assets as BioNFTs™ and earn from every commercial use. Starting with 23andMe genotype data, we're expanding to whole exome and genome sequencing.
Metric | Grail (Traditional) | GenoBank Grail 3.0 |
---|---|---|
Patient Compensation | $0 | $188-375 per patient (15% of $1,250-2,500) |
Data Control | Corporate owned | Patient owned via BioNFT™ |
Exit Value Distribution | 0% to patients | 15% minimum to patients |
Secondary Market | None | Liquid on DEX |
AI Training Transparency | Hidden | Full Story Protocol visibility |
Commercial License Secured: We've secured dbNSFP commercial licensing (normally $10,000/year) to provide hospital-grade variant annotation at consumer prices ($5-10/analysis). This transforms raw sequences into clinically actionable insights.
50-patient pilot at major medical institution with dual-track validation - traditional records plus patient-owned BioNFTs™
Whole exome sequencing with dbNSFP annotation - a major step up from 23andMe genotyping to clinical-grade genomic data that drives treatment decisions
15% royalty on all commercial use, automatically distributed via smart contracts to BioNFT™ holders
Scenario | Traditional Model | GenoBank.io™ + Story |
---|---|---|
Company Sale | All data transferred | BioNFT™ remain with patients |
New AI Model | Uses data without asking | Must license from owners |
AI Training | Hidden, uncompensated | Transparent, paid |
Exit Rights | None | Instant liquidity |
AI Revenue Share | 0% | 15% guaranteed |
Metric | Traditional Biobank | BioNFT™ AI Asset |
---|---|---|
Initial Value | $0 (donated) | $1,300 (£1,000) |
Annual Yield | $0 | $130-390 (£100-300) |
Liquidity | None | Instant (DEX) |
Collateral Value | $0 | $650-910 (£500-700) |
Governance Rights | None | Vote on AI uses |
Exit Options | None | Sell, stake, lend |
Pharmaceutical companies need diverse genomic data to train models that predict drug efficacy and side effects across populations
Healthcare AI systems require genomic training data to personalize treatments based on individual genetic variations
Early detection models need massive genomic datasets to identify disease patterns years before symptoms appear
Public health AI requires diverse genomic data to understand disease spread and develop targeted interventions
Major AI companies are building healthcare models with limited, biased datasets because they can't access the 547M genomes locked in corporate silos. GenoBank.io™ solves this by making genomic data programmable, licensable, and accessible through Story Protocol—while ensuring patients get paid for every use.
Tech giants need quality training data
GDPR/CCPA demanding consent frameworks
Infrastructure for programmable IP
Patients demanding AI revenue share
By 2027, GenoBank.io™ and Story Protocol will unlock $975M in AI training value from just 375,000 genomic datasets— creating the first patient-owned AI training marketplace where data creators finally get paid.
While tech giants scramble for AI training data, 547 million genomes sit locked away.
It's time to unlock them as programmable AI assets on Story Protocol.