MULTIOMICS™
The engine that predicts disease 8 weeks before clinical manifestation — by measuring the velocity delta between your gut and blood.
BURAK analyzes 7 layers of biological data. The magic is in the velocity difference — when blood markers change fast but gut stays stable, disease is coming.
What's happening: Blood markers spiking but gut hasn't changed yet
Meaning: Acute metabolic stress — body is compensating
→ 8-week warning triggered
What's happening: Both systems deteriorating together
Meaning: Chronic condition developing — systemic issue
→ Intervention needed now
What's happening: Both systems in balance
Meaning: Healthy metabolic state
→ Continue monitoring
What's happening: Gut dysbiosis present but blood stable
Meaning: Early stage — blood will follow in 4-8 weeks
→ Gut intervention window
This is why we track 45 markers across 7 layers — single markers lie, patterns don't.
The GUT moves slowly (weeks/months). BLOOD moves fast (hours/days). INFLAMMATION amplifies everything. By measuring the velocity difference between these layers, BURAK predicts metabolic failure 8 weeks before clinical manifestation.
Click any node to trigger the cascade. Watch how dysbiosis propagates through the system — and where insurance intervention saves millions.
Based on the research we're applying, here's what BURAK aims to achieve.
We're moving into production. We want to understand your workflow — and in return, offer you a free pilot program to see the results firsthand.
Insurance Companies • TPAs • Self-Insured Employers
Potential ROI per 1,000 members:
(Exact figures to be validated in pilot)
Hospitals • Government Health • Clinics • Health Systems
Goal per patient cohort:
(Based on peer-reviewed research)
We're looking for partners to validate our approach. In exchange for helping us understand your workflow, we'll run a free pilot on a cohort of your patients — so you can see the results before any commitment.
We take data privacy seriously. Our production pipelines are being deployed on Google Cloud Healthcare Containers — built for HIPAA compliance and healthcare-grade security.
Connect with Waseem Ahmad Ahanger on LinkedIn
No commitment required. Let's explore together.
A group of engineers and scientists building tools to apply breakthrough research in clinical practice.
Our mission: Take peer-reviewed scientific research and build practical tools that clinicians and health systems can actually use.
BURAK is built on peer-reviewed gut-metabolic axis research. Here's how we're applying these scientific findings.
Studies show dysbiosis (gut imbalance) precedes metabolic disease by weeks to months. Changes in F/B ratio and Akkermansia levels correlate strongly with future T2DM, CVD, and NAFLD.
Research demonstrates that inflammatory markers (CRP, IL-6) amplify the gut-blood connection. Patients with elevated inflammation show 5-6× higher progression rates to clinical disease.
The key insight from the research: gut markers change slowly (weeks/months) while blood markers change quickly (days/weeks). When blood markers spike but gut markers remain stable, it indicates acute metabolic stress — a predictive window before clinical disease manifests.
We gather the biomarkers identified in the research: gut microbiome, blood metabolics, inflammation
We measure the rate of change in each layer and calculate the velocity delta as described in research
When velocity delta exceeds research-defined thresholds, we flag for early intervention
Here's how the velocity calculation would work based on the research parameters:
What This Means: If the research is correct, a velocity delta of 12.43 (above the 8.0 threshold) would indicate elevated risk approximately 8 weeks before clinical symptoms appear.
Based on published studies, these biomarker patterns show strong correlations with disease outcomes. BURAK tracks these relationships to identify at-risk individuals.
BURAK applies findings from 3+ years of peer-reviewed gut-metabolic research approved by healthcare scientific committees. We're building tools to make this research actionable in clinical practice.