Test Price
25,000 AED✅ Home Collection Available
Cattle Genome Sequencing (30X Coverage) in UAE | 25000 AED | 2026 DHA Guidelines
تحليل تسلسل الجينوم البقري (30X) في الإمارات | 25000 درهم | معتمد من هيئة الصحة بدبي
Accuracy Guarantee: 99.9% Base Call Accuracy (Q30 > 90%) via ISO 9001:2015 Certified NGS Labs.
Premium Logistics: Paid Hospital-Grade Home Collection (Whole Blood) with ISO‑Certified Cold‑Chain Transport.
Clinical Guidance: Telephonic Post‑Analysis Consultation with PhD‑level Genomics Researchers.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
الملخص التنفيذي
ضمان الدقة: دقة استدعاء القاعدة 99.9٪ وجودة عمليات تسلسل الجيل التالي معتمدة بمعيار الآيزو 9001:2015. الخدمات اللوجستية المتميزة: سحب دم منزلي على مستوى المستشفى ونقل مبرد معتمد. استشارة هاتفية بعد التحليل من باحثين متخصصين في علم الجينوم. تحقق من التغطية التأمينية مباشرة عبر واتساب +971 54 548 8731.
Overview
Whole‑genome sequencing of bovine (cattle) samples at 30X coverage delivers high‑resolution genomic maps for comparative oncology, genetic trait mapping, and zoonotic disease research. The test utilizes extracted DNA or whole blood, processed via validated Illumina NovaSeq 6000 with ISO‑accredited bioinformatics pipelines to ensure research‑grade data integrity.
| Feature | Our Test (30X NGS) | Closest Alternative (Sanger) |
|---|---|---|
| Precision | 30X uniform coverage; SNV sensitivity > 99.5% | Targeted regions only; no broad genome profiling |
| Methodology | NGS (Illumina NovaSeq) + Q30 QC | Capillary sequencing |
| Turnaround Time | 5 weeks | 6–8 weeks for equivalent coverage (by synthesis) |
Physician Insight & Safety Protocol
“This bovine whole‑genome analysis is a powerful research tool for cross‑species translational studies. The 30X depth allows reliable variant detection for trait mapping and oncological model development, but all findings must be correlated with phenotypic data and validated in the intended experimental context.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
Medication Warning:
Do not discontinue any prescribed medication or alter any animal husbandry protocol without consulting your veterinarian or research supervisor. This genomic is not a diagnostic assay and should not guide immediate therapeutic changes.
Exclusion Criteria & Emergency Red Flags
- Sample Exclusion: Extracted DNA with concentration < 50 ng/µL, A260/A280 ratio outside 1.8–2.0, or evidence of degradation.
- Whole Blood Rejection: Hemolysis, clotting, or collection in non‑EDTA tubes will invalidate the run.
- Emergency Red Flag:
- Immediately report any accidental breakage of collection tubes containing blood or DNA to our biosafety team at +971 54 548 8731. Do not handle spilled biological material without appropriate PPE.
Frequently Asked Questions (Clinical & Research Guidance)
1. What depth of coverage does “30X” guarantee, and why is it important for my research?
30X coverage means each base in the cattle genome is sequenced an average of 30 times, providing a >99.9% base call accuracy and robust detection of single‑nucleotide variants essential for reliable comparative oncology and genetic mapping studies.
2. ما المدة الزمنية اللازمة لصدور النتائج وهل تتوفر خدمة الاستشارة بعد التحليل؟
مدة إنجاز التحليل هي 5 أسابيع اعتباراً من استلام العينة المطابقة للمعايير، ويُقدم فريق الدعم الاستشاري جلسة هاتفية مجانية بعد إصدار التقرير لتفسير البيانات الجينومية والإجابة عن استفسارات الباحثين.
3. Can I submit extracted DNA or only whole blood, and how should I prepare the sample?
Both high‑quality extracted DNA (≥2 µg, OD 260/280 1.8–2.0) in TE buffer and whole blood collected in EDTA tubes are accepted; extracted DNA requires cold shipping on dry ice while whole blood must be refrigerated and processed within 48 hours for optimal sequencing yield.
Facility License No. 9834453 | ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139)
Support & Booking: +971 54 548 8731
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التحقق من التغطية التأمينية
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