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22,500 AED

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Whole Genome Sequencing (30X) & Variant Calling in UAE | 22500 AED | 2026 DHA Guidelines

تحليل تسلسل الجينوم الكامل (30X) في الإمارات | 22500 درهم | معتمد من هيئة الصحة بدبي

ملخص تنفيذي: يوفر هذا الاختبار التشخيصي المتقدم تحليلاً شاملاً للجينوم البشري بتغطية 30 ضعفًا، وفقًا لأعلى معايير الجودة والتشريعات الصحية الإماراتية لعام 2026. يُضمن تشخيص الأمراض الوراثية والسرطانية بدقة استثنائية وخصوصية تامة للبيانات، مع خدمة سحب منزلي فاخرة ومتابعة سريرية هاتفية بعد النتيجة.

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
  • Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy (8 AM–11 PM).
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance with a DHA-licensed genetic specialist to interpret results.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Clinical Overview

Whole Genome Sequencing (WGS) with 30X depth offers the most comprehensive analysis of all human genes simultaneously, identifying pathogenic single nucleotide variants (SNVs), indels, copy number variations (CNVs), and structural rearrangements. This test is designed for oncology predisposition screening, rare disease diagnosis, and proactive health management, processed at a DHA-licensed UAE facility under strict data privacy.

Comparison Table

Feature Our Test (WGS 30X) Closest Alternative (WES/Clinical Exome)
Genomic Coverage Entire genome (coding + non-coding) ~2% coding regions only
Variant Detection Accuracy 99.9% for SNVs, CNVs, SVs High for exonic SNVs; misses SVs/non-coding
Turnaround Time 8 weeks 6–10 weeks
Methodology NGS (Illumina, 30X depth), ISO-Validated NGS (Varies)

Physician Insight & Safety Protocol

Dr. PRABHAKAR REDDY (DHA: 61713011):

“As a clinical geneticist, I emphasize that whole genome sequencing is a powerful but complex tool. Results must always be correlated with your personal and family medical history. A variant of unknown significance should never be confused with a confirmed diagnosis.”

⚠️ Critical Medication Warning

Do not discontinue prescribed medication or alter treatment plans based solely on genetic results without consulting your treating physician.

Safety & Exclusion Criteria

  • Exclusion: Individuals unable to provide informed consent (per UAE Federal Decree-Law No. 41 of 2024). Minors require guardian consent per CDS 2026 regulations.
  • Exclusion: Patients with active hematological malignancies may have altered germline DNA (consult specialist).
  • ER Red Flags: If genetic report indicates a high-risk cancer syndrome, immediate oncological consultation is required – do not delay. Report any new unexplained symptoms to your doctor without waiting for genetic counsellor availability.
  • Data privacy is guaranteed under UAE PDPL; your genomic data will not be shared without explicit consent.

Patient FAQ & Clinical Guidance

Q: What exactly does “30X coverage” mean for my genome?

Snippet: 30X coverage means each DNA letter is read 30 times on average, ensuring >99.9% accuracy in detecting even subtle genetic variants linked to hereditary cancers and rare diseases.

س: كيف أستعد لاختبار الجينوم الكامل؟

Snippet: لا يحتاج الاختبار إلى صيام، لكن يُنصح بشرب الماء لتسهيل سحب عينة الدم (5 مل) عبر خدمة السحب المنزلي، مع إبلاغك عن أي أدوية مميعة للدم تتناولها لتجنب خطر النزيف.

Q: Will my insurance cover the 22500 AED cost?

Snippet: Many UAE insurance plans cover whole genome sequencing when medically indicated; we verify your eligibility directly via WhatsApp at +971 54 548 8731 and handle pre-approval paperwork on your behalf.

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توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.

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