We are entering a new era of personalized health. Instead of a one-size-fits-all approach, we can now unlock the unique instruction manual inside every individual: the human genome. Hayat + harnesses the sequencing power and helps translate your genetic data into actionable strategies for a healthier, stronger, and more optimized life. It’s proactive life management, decoded from your DNA.
Think of your genome as the body’s complete instruction manual. This manual is written in a code called DNA, composed of four letters (A, T, C, G). Genes are the specific instructions within this manual, dictating everything from eye color to how you process food.
While all humans share 99.9% of their DNA, the tiny fraction that differs is what makes you unique. These natural genetic variations are not defects; they are the source of human diversity and influence your health, physical traits, and predispositions to certain conditions.
A single variation in your genetic code can have a significant impact. It can influence your risk for conditions like heart disease or cancer, how your body responds to medications, and even your innate athletic abilities. Hayat + bridges the gap between this code and its real-world consequences.
Proactive Prevention: Identify hereditary risks for cancer and cardiovascular conditions early, allowing for personalized screening and prevention strategies.
Informed Family Planning: Learn your carrier status for over 200 inherited conditions to make informed decisions when planning a family.
Understand how your body will respond to common medications, avoiding adverse reactions and ensuring effective treatment from the start.
For rare or undiagnosed conditions, a single test may provide a definitive diagnosis, ending years of uncertainty and misdiagnosis.
Tailored Training: Discover your genetic predisposition for power or endurance to customize training regimens that maximize your natural strengths.
Strategic Nutrition: Optimize your diet based on how your body metabolizes nutrients and your specific needs for vitamins and minerals.
Injury Prevention: Ongoing research can help identify genetic risks for tendon and ligament injuries to implement targeted prevention and recovery strategies, keeping you at peak performance.
Ongoing research will help identify genetic markers associated with resilience to physical and psychological stress, allowing for preemptive support and targeted training for high-stakes roles.
Screen for genetic hyper susceptibility to specific workplace hazards, ensuring personnel are not placed in harmful environments.
A healthier, more resilient force leads to greater mission success, reduced medical expenditures, and lower downstream costs.
A deep, targeted analysis of your exome—the protein-coding regions of your genome. WES is a powerful and efficient tool for clinical diagnostics, ideal for those with a suspected inherited disorder or a specific clinical question. It provides high-resolution insight into the most functionally important part of your DNA.
An innovative hybrid that combines the depth of WES with the breadth of WGS. BGE delivers a high-resolution analysis of your protein-coding genes while also providing a genome-wide view to detect large-scale structural changes. It offers a comprehensive, cost-effective analysis that captures both fine details and the big picture.
The ultimate exploration of your genetic code. WGS provides the most complete and definitive view of your entire genome, including both coding and non-coding regions. It is the gold standard for solving complex medical mysteries and provides a future-proof health asset that can be re-analyzed as science evolves.
Choose the right genomic testing solution for your needs
| Feature / Capability | Hayat + WES | Hayat + BGE | Hayat + WGS |
|---|---|---|---|
| Technical Specifications | |||
| Genome Coverage | ~2% (Protein-coding regions) | Blended (~2% deep, >98% shallow) | >98% (Entire Genome) |
| Detects Common Variants (SNPs) | ✓ | ✓ | ✓ |
| Detects Rare Variants in Genes | ✓ | ✓ | ✓ |
| Detects Copy Number Variants (CNVs) | ✓ | ✓ | ✓✓ (Superior) |
| Detects Structural Variants (SVs) | Limited | Limited | ✓ |
| Detects Repeat Expansions | ✗ | ✗ | ✓ |
| Detects Non-Coding Variants | ✗ | Limited | ✓ |
| Clinical & Diagnostic Applications | |||
| Diagnosis for Rare/Undiagnosed Disease | ✓ | ✓ | ✓✓ |
| Ending the "Diagnostic Odyssey" | Recommended | Recommended | Gold Standard |
| Feature / Capability | Hayat + Baseera WES | Hayat + Shamil BGE | Hayat + Kamal WGS |
| Proactive Health & Wellness | |||
| Carrier Screening (Family Planning) | ✓ | ✓ | ✓✓ |
| Pharmacogenomics (Drug Response) | ✓ | ✓ | ✓✓ |
| Proactive Risk (Cancer, Cardiac) | ✓ | ✓ | ✓✓ |
| Wellness & Lifestyle Traits | Limited | ✓ | ✓ |
| Performance & Occupational Applications | |||
| Foundational Athletic Traits (e.g., ACTN3) | ✓ | ✓ | ✓ |
| Advanced Injury Risk (e.g., Collagen Genes) | ✓ | ✓ | ✓ |
| Comprehensive Performance Profile | ✗ | ✗ | ✓ |
| Occupational Health Screening | ✓ | ✓ | ✓✓ |
| Resilience & Stress Marker Analysis | ✗ | Limited | ✓ |
Your genome is your personal instruction manual. Sequencing ensures that we can read it. This knowledge is not about fate; it’s about empowerment. It provides the foresight to prevent disease, the insight to optimize performance, and the wisdom to build a more resilient life.
Precision Diagnostics. Trusted Results. Healthier Tomorrow.
Sharjah – 506 & 507 Fifth Floor, Al Faisal 2 Building, Qutadah Bin Al Nua’man Street, Postal Code — 61157, Al Nad, Al Qasimia, Sharjah
Copyright © 2025 All Rights Reserved.
