Test Price
6,500 AED✅ Home Collection Available
NGS Whole Exome for Couple Test in UAE | 6,500 AED
Executive Summary & Core Metrics
NGS Whole Exome Sequencing for couples delivers a comprehensive genetic risk assessment for recessive disorders, with analytical sensitivity exceeding 99.9% for single nucleotide variants and small indels. The service includes:
- Accuracy: 99.9% analytical sensitivity via ISO‑15189 accredited laboratory processes.
- Logistics: VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection available daily from 8 AM to 11 PM.
- Post‑test Support: Telephonic genetic counselling and result interpretation.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
Whole Exome Sequencing (WES) targets the protein‑coding regions of the genome—about 1–2% of the total—where the majority of known disease‑causing variants reside. The test simultaneously analyses both partners’ exomes to identify shared pathogenic variants that could increase the risk of autosomal recessive and X‑linked disorders in their offspring.
| Feature | Our Test (Precision/Method/Speed) | Closest Alternative |
|---|---|---|
| Precision | 99.9% analytical sensitivity for SNVs/indels | ~95% (targeted mutation panel) |
| Method | NGS Whole Exome Capture (Illumina NovaSeq) | Standard Carrier Screening (genotyping) |
| Speed (TAT) | 3–4 weeks | 2–3 weeks |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
“NGS Whole Exome Sequencing for couples is a powerful screening tool, but its results must always be interpreted within the clinical context and paired with comprehensive genetic counselling. No medication should be altered without consulting the prescribing physician. Incidental findings require careful clinical correlation before any action is taken.”
Safety Advisory
- Do not discontinue any prescribed medication without explicit instruction from your physician.
- If you experience excessive bleeding, large haematoma, or signs of systemic allergic reaction after sample collection, seek immediate medical attention.
Exclusion Criteria
- Known pregnancy (alternative non‑invasive screening methods are available).
- Active bleeding disorders or severe anaemia that may compromise venous access.
- History of allergic reaction to blood draw procedures.
Patient FAQ & Clinical Guidance
1. What is NGS Whole Exome for Couples, and who should consider it?
NGS Whole Exome Sequencing for couples screens both partners for shared genetic variants that could cause severe recessive conditions in children. It is recommended for couples planning pregnancy—especially those with a family history of genetic disorders, consanguineous marriages, or previous affected pregnancies.
2. How accurate is the test, and what does a negative result mean?
With >99.9% sensitivity for single nucleotide variants and small insertions/deletions, this test is highly accurate. A negative result reduces the carrier risk but does not eliminate it entirely—variants in non‑coding regions or large structural rearrangements may not be detected, so residual risk remains.
3. What is the process for sample collection, and how long does it take?
A 5 mL blood sample is collected from each partner at your home by our VIP Mobile Phlebotomy team, using temperature‑controlled cold‑chain logistics. Results are typically ready in 3–4 weeks. You will receive secure online access to your report, followed by a telephonic consultation with a genetic counsellor.
UAE Regulatory & Data Privacy Adherence
Compliance with UAE Law
- All genetic data are processed in accordance 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.
- Clinical safety and patient consent follow the provisions of Federal Decree‑Law No. 4 of 2016 on Medical Liability.
- Laboratory is operated under DHA Facility License 1143 and ISO 15189:2012 standards.
Clinical & Logistical Metadata
| Test Name | NGS Whole Exome for Couple Test |
| Price (AED) | 6,500 |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral whole blood (5 mL per partner) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Daily 8 AM–11 PM) |
| Methodology Used | Next‑Generation Sequencing (Whole Exome Capture) on Illumina NovaSeq platform |
| ICD-10-CM Code | Z13.89 (encounter for screening for other genetic disorders) |
| LOINC Code | 101297-1 (Exome sequencing panel) |
| DHA Facility License & Laboratory Address | DHA License 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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