Test Price
35,000 AED✅ Home Collection Available
MiSeq 2×250 Paired-End Sequencing in UAE | 35,000 AED | DNA Labs UAE
Executive Summary & Core Metrics
Clinical-Grade Accuracy. Premium Logistics. Full Regulatory Compliance.
- 99.9% Diagnostic Sensitivity – Assured by ISO 9001:2015 accredited NGS processing.
- VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection – ISO-certified logistics service available daily from 8 AM to 11 PM.
- Post-Test Clinical Guidance – Dedicated telephonic consultation with a DHA-licensed specialist to interpret your results.
- Direct Insurance Billing – WhatsApp pre‑verification at +971 54 548 8731.
Price
35,000 AED
TAT: 14 days
Test Overview & Methodology
This high-depth DNA sequencing assay employs the Illumina MiSeq platform with 2×250 paired-end chemistry to deliver ultra‑accurate genomic data. The test is ideally suited for oncology profiling, rare‑disease gene discovery, and biobank sample validation. Each sample undergoes stringent quality control metrics and bioinformatic variant calling aligned with international clinical guidelines.
| Feature | Our Test – MiSeq 2×250 | Closest Alternative (Amplicon / Sanger) |
|---|---|---|
| Read Length & Precision | 2×250 bp paired-end, >99% raw accuracy | Single‑end 500 bp, moderate accuracy |
| Methodology | Illumina NGS with bioinformatic variant calling | Sanger sequencing / targeted amplicon panels |
| Turnaround Time | 14 days | 4–6 weeks |
| Clinical Coverage | Whole genome / exome / large panels | Single genes or small hotspot regions |
Physician Insight & Safety Protocols
From Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403: “Genomic sequencing provides a powerful window into your inherited health risks and treatment options. I encourage every patient to discuss the scope of this test—including incidental findings—with a qualified genetic counselor before proceeding. No treatment decision should be made solely on raw sequencing data; always integrate results with your complete clinical history.”
Clinical Advisory & Pre-Test Counseling
A mandatory pre-test consultation with a DHA-licensed genetic professional is strongly recommended for all patients undergoing comprehensive sequencing. This session covers the scope of the analysis, potential secondary findings, data storage policies, and implications for family members. Written informed consent in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability must be documented prior to sample collection.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Known bleeding diathesis (coagulopathy) that cannot be corrected prior to blood draw; severe anemia (Hb <8 g/dL) for venous collection; active local infection at venipuncture site.
- Emergency Red Flags: If after sample collection you develop extensive bruising, persistent bleeding, dizziness, or signs of infection (redness, warmth, pus), seek immediate medical attention.
- Home collection is performed by licensed phlebotomists under ISO cold‑chain protocol; however, in case of any adverse event, call the emergency contact provided with your appointment confirmation.
Patient FAQ & Clinical Guidance
1. What is the turnaround time for MiSeq sequencing results?
Patients receive their comprehensive, clinically annotated report within 14 days of sample receipt, enabling timely oncological or genetic counseling decisions. The laboratory processes samples on a dedicated flow cell and performs rigorous bioinformatic validation. For urgent cases, a preliminary verbal briefing can be arranged after the first week.
2. What sample types are accepted for this sequencing test?
We accept both high-quality extracted DNA (concentration ≥20 ng/µL, A260/280 1.8–2.0) and whole blood collected in EDTA tubes, which is then processed in our BSL-2 accredited facility. Whole blood ensures maximal genomic integrity; if you opt for extracted DNA, a specialized courier kit will be dispatched to your home for safe transfer.
3. How is home collection arranged for this genetic test?
Our VIP Mobile Phlebotomy service dispatches a licensed phlebotomist to your residence within a scheduled window between 8 AM and 11 PM daily. All samples are transported using temperature-controlled cold-chain logistics with real-time GPS monitoring. Blood collection in EDTA tubes is performed under aseptic conditions, and the sample is delivered to our Dubai Healthcare City laboratory within 4 hours of collection.
UAE Regulatory & Data Privacy Adherence
Data Protection & Legal Framework
This diagnostic service operates 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. All genomic sequence data are encrypted end-to-end and stored exclusively on Dubai-based servers with restricted access protocols. No raw data is transferred outside the UAE without explicit patient consent documented through a separate data processing addendum.
The laboratory holds ISO 9001:2015 accreditation under certificate INT/EGQ/2509DA/3139 and adheres to the DHA Standards for Clinical Laboratories. Patients retain the right to access, rectify, and request deletion of their personal data in accordance with PDPL Article 12. For data subject requests, contact our Data Protection Officer at privacy@dnalabsuae.com.
Clinical & Logistical Metadata
| Test Name | MiSeq 2×250 Paired-End Sequencing |
| Price (AED) | 35,000 AED |
| Turnaround Time | 14 business days (2 weeks) |
| Sample Type / Matrix | Whole Blood (EDTA) or High-Quality Extracted DNA (≥20 ng/µL) |
| Methodology Used | Illumina NGS with 2×250 paired-end chemistry and bioinformatic variant calling |
| ICD-10-CM Code | Z01.818 |
| LOINC Code | 81247-9 |
| DHA Facility License & Address | License 1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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