Test Price
4,500 AED✅ Home Collection Available
Whole Genome Sequencing & Variant Calling (10X Genomics) in UAE – 4500 AED – DHA Licensed
Executive Summary & Core Metrics
Clinical Accuracy:
99.9% diagnostic sensitivity via ISO 9001:2015 certified processing (Cert: INT/EGQ/2509DA/3139), leveraging 10X Genomics linked‑read technology and validated variant calling pipelines.
Premium Logistics:
VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection. Available daily from 8 AM to 11 PM, ensuring sample integrity from your doorstep to our DHA‑licensed facility.
Post‑Test Guidance:
Telephonic clinical interpretation of results by DHA‑credentialed specialists – we bridge the gap between complex genomic data and actionable health decisions.
Insurance Support:
Direct Billing Verification via WhatsApp: +971 54 548 8731
Test Overview & Methodology
Whole Genome Sequencing (WGS) with 10X Genomics linked‑read technology delivers phased, high‑resolution genomic data, enabling precise variant calling for hereditary cancer syndromes, anti‑aging pharmacogenomics, and rare disease research. Every report is aligned with DHA genomic reporting standards and international guidelines.
| Feature | Our 10X WGS Test | Closest Alternative |
|---|---|---|
| Precision | 99.9% diagnostic sensitivity | ~98.5% for standard short‑read WGS |
| Method | Linked‑Read WGS (10X Chromium™) + AI variant calling | Conventional short‑read WGS (Illumina only) |
| Turnaround | 8 weeks (accelerated reporting available) | 10–12 weeks |
Physician Insight & Safety Protocols
“Genomic results represent a foundational layer of your health narrative, not a final diagnosis. I integrate these findings with your personal and family medical history, lifestyle factors, and clinical examination to formulate a comprehensive, individualized care plan. This test empowers you with information, but it should always complement—not replace—ongoing dialogue with your primary physician.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
⚠️ Medication Advisory
Do not discontinue any prescribed medication, including chemopreventive or anti‑aging therapies, without direct consultation with your supervising physician.
Exclusion Criteria & Emergency Red Flags
- Individuals without pre‑test genetic counselling by a DHA‑licensed professional (mandatory for minors per UAE Federal Law No. 2 of 2019).
- Pregnant patients requiring actionable prenatal findings must be referred to a maternal‑fetal medicine specialist before sampling.
- RED FLAG: If the report reveals a high‑penetrance pathogenic variant (e.g., BRCA1/2, TP53), an urgent oncology consultation must be arranged; do not delay preventive measures.
- RED FLAG: Incidental findings indicating imminent cardiac risk (e.g., RYR2, KCNQ1) require immediate cardiology evaluation and family cascade screening.
Patient FAQ & Clinical Guidance
1. How does 10X linked‑read sequencing improve variant calling compared to standard WGS?
Linked‑read technology preserves long‑range genomic context, enabling phasing of haplotypes, resolution of complex structural variants, and mapping of repeats – critical for accurate cancer predisposition and anti‑aging gene assessment.
2. What conditions are covered in the report and how are they prioritised?
Our curated gene panel focuses on actionable hereditary cancer syndromes (ICD‑10‑CM Z15.09, Z14.8), cardiovascular susceptibility (Z13.79), and pharmacogenomic markers for anti‑aging protocols. Clinically significant findings are flagged immediately for genetic counselling.
3. Is home collection safe for a genomic test with such strict cold‑chain requirements?
Our phlebotomists use ISO‑validated temperature‑controlled kits and real‑time monitoring. DNA extraction from whole blood or pre‑extracted DNA is stabilised within minutes, guaranteeing sample integrity until processing in our DHA‑licensed genomic lab.
UAE Regulatory & Data Privacy Adherence
All services comply with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Patient consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Your genomic data is encrypted, access‑controlled, and processed solely for diagnostic purposes with your explicit written consent.
Clinical & Logistical Metadata
| Test Name | Whole Genome Sequencing & Variant Calling (10X Genomics) |
| Price (AED) | 4,500 |
| Turnaround Time | 8 weeks (accelerated reporting available) |
| Sample Type / Matrix | Whole blood (peripheral) or pre‑extracted DNA |
| Methodology Used | 10X Chromium linked‑read sequencing + AI‑powered variant calling |
| ICD‑10‑CM Code | Z15.09, Z14.8 |
| LOINC Code | 10520-0 |
| DHA Facility License & Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians