Test Price
22,500 AEDโ Home Collection Available
Whole Genome Sequencing (30X Coverage) & Variant Analysis in Dubai UAE | 22,500 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% diagnostic sensitivity for single nucleotide variants, insertions/deletions, copy number variations, and structural rearrangements via ISO 9001:2015 accredited processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM for standard peripheral whole blood specimens.
- Clinical Guidance: Post-test telephonic consultation with a DHA-licensed Consultant Medical Geneticist to interpret all reported variants and formulate a personalized management plan.
- Insurance Concierge: Direct billing verification and pre-approval handled via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
Whole Genome Sequencing (WGS) at 30X average depth interrogates the entirety of the human genome โ both coding and non-coding regions โ enabling simultaneous detection of pathogenic single nucleotide variants (SNVs), small insertions and deletions (indels), copy number variations (CNVs), and large structural rearrangements. This comprehensive test is indicated for hereditary cancer predisposition screening, rare disease diagnostic workup, pharmacogenomic profiling, and proactive health optimization. All processing occurs at a DHA-licensed laboratory facility in Dubai Healthcare City under stringent quality control and data privacy protocols aligned with UAE federal law.
| Feature | Our Test (WGS 30X) | Closest Alternative (Clinical Exome / WES) |
|---|---|---|
| Genomic Coverage | Entire genome โ coding regions, non-coding regulatory elements, intronic regions, and intergenic sequences | Approximately 2% of the genome (exonic regions only) |
| Variant Classes Detected | SNVs, indels, CNVs, structural variants, mitochondrial variants | Primarily exonic SNVs and small indels; limited CNV detection |
| Turnaround Time | 8 weeks | 6โ10 weeks depending on capture and analysis complexity |
| Methodology | Next-Generation Sequencing on Illumina platform at 30X mean depth, ISO-validated bioinformatics pipeline | Next-Generation Sequencing with hybridization capture; variable depth |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
โWhole genome sequencing provides an unprecedented breadth of genetic data, but clinical interpretation requires careful correlation with each patientโs personal and family medical history. A variant of uncertain significance should never be equated with a disease-causing mutation. I always advise patients to review their results in a dedicated genetic counselling session before making any medical decisions.โ
Critical Advisory โ Medication & Treatment Continuity
Do not discontinue any prescribed medication, alter drug dosages, or modify your treatment plan based solely on genetic findings without explicit guidance from your treating physician. Genetic results are one component of a comprehensive clinical assessment and must be integrated with physical examination, biochemical markers, and imaging data.
Safety & Exclusion Criteria
- Informed Consent: Individuals who are unable to provide valid informed consent in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability are excluded. For minors, written consent from a legal guardian is mandatory.
- Hematological Malignancy Caution: Patients with active hematological malignancies (e.g., leukemia, lymphoma) may have altered germline DNA in peripheral blood; consultation with a hematologist is advised before proceeding with WGS from a blood specimen.
- Emergency Red Flags: If the genetic report identifies a high-penetrance cancer predisposition syndrome (e.g., TP53, BRCA1/2, MLH1, MSH2), immediate referral to the relevant oncology or genetics specialist is required. Do not delay seeking medical attention for new or unexplained symptoms while awaiting a genetic counselling appointment.
- All genomic data is processed and stored under the protections of 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. Your data will not be shared with third parties without your explicit written consent.
Patient FAQ & Clinical Guidance
1. What does โ30X coverageโ mean for the accuracy of my genome report?
30X coverage indicates that each nucleotide in your genome is sequenced an average of 30 independent times. This depth achieves >99.9% sensitivity for detecting single nucleotide variants, small insertions and deletions, and copy number alterations, ensuring that clinically significant findings are not missed due to sequencing stochasticity.
2. How should I prepare for the whole genome sequencing blood draw?
No fasting is required for the collection of the 5 mL whole blood sample in an EDTA tube. You are encouraged to stay well hydrated to facilitate venipuncture. Please inform our phlebotomist of any anticoagulant or antiplatelet medications you are currently taking so that appropriate precautions can be observed. Our VIP Mobile Phlebotomy service is available from 8 AM to 11 PM daily.
3. Will my health insurance cover the 22,500 AED cost for whole genome sequencing?
Many UAE-based health insurance plans provide coverage for whole genome sequencing when it is medically indicated โ for example, in the diagnostic workup of suspected genetic disorders or for high-risk cancer predisposition screening. Our team verifies your eligibility and manages the pre-approval documentation on your behalf. Please send your policy details via WhatsApp to +971 54 548 8731 for a preliminary coverage assessment.
UAE Regulatory & Data Privacy Adherence
All genomic testing, data handling, and reporting procedures at DNA Labs UAE are conducted in full compliance 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 genomic data is encrypted, access-controlled, and never shared with external parties without explicit written authorization. The laboratory holds DHA Facility License Number 1143 and operates under the regulatory oversight of the Dubai Health Authority and the UAE Ministry of Health and Prevention.
Clinical & Logistical Metadata
| Test Name | Whole Genome Sequencing (30X Coverage) with Comprehensive Variant Calling |
| Price (AED) | 22,500 AED |
| Turnaround Time | 8 weeks from sample receipt at laboratory |
| Sample Type / Matrix | Peripheral whole blood (5 mL in EDTA tube); VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM |
| Methodology Used | Next-Generation Sequencing (Illumina platform, 30X mean depth) with ISO-validated bioinformatics analysis for SNV, indel, CNV, and structural variant detection |
| ICD-10-CM Code | Z13.89 |
| LOINC Code | 90515-2 |
| DHA Facility License & Laboratory Address | DHA Facility License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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