Whole Genome Sequencing tests in Dubai & UAE

Compare available Whole Genome Sequencing tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

6,000.00–30,000.00 AED

Clinical preparation

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Whole Genome Sequencing test prices

Showing 1–6 of 6 matching tests.

Whole Genome Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-191 Bacterial Genome De Novo Assembly and Annotation (Illumina & ONT Hybrid) Test This diagnostic test evaluates the complete genetic sequence of a bacterial isolate.	Pure bacterial culture	4 weeks	6,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Complete bacterial genome sequence", "Antimicrobial resistance genes", "Virulence factors", "Strain relatedness"] Parameters [] Preparation ["Bacterial culture must be grown prior to submission.", "Antibiotics should ideally be withheld only if clinically safe to do so."] Indications ["Outbreak tracing", "Antimicrobial resistance gene profiling", "Pathogen discovery", "Complex or difficult-to-treat infections"] Measurement technique Confirm with laboratory Codes LOINC: 65297-9 ICD-10: B96.8 Clinical summary This diagnostic test evaluates the complete genetic sequence of a bacterial isolate.
TEST-300 Bacterial Genome Sequencing, De Novo Assembly and Annotation (Illumina and ONT Hybrid) Test This test provides a complete genomic sequence of bacteria, identifying species, antibiotic resistance, and virulence factors.	Whole blood (EDTA) or extracted DNA	8 weeks from accepted sample	17,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Bacterial species identification", "Antibiotic resistance genes", "Virulence factors", "Functional annotation"] Parameters [] Preparation [] Indications ["Pathogen surveillance", "Strain typing", "Microbiome research", "Infection outbreak tracking", "Personalized microbiome studies"] Measurement technique Confirm with laboratory Codes LOINC: 60521-0 ICD-10: Z01.89 Clinical summary This test provides a complete genomic sequence of bacteria, identifying species, antibiotic resistance, and virulence factors.
TEST-295 Cattle Genome Sequencing and Variant Calling (10X) Test This test performs whole genome sequencing on bovine samples to identify genetic variants.	Whole Blood	8 weeks	30,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genetic variants", "Structural variants", "Long-range haplotypes"] Parameters [] Preparation [] Indications ["Livestock genetic research", "Zoonotic disease modelling", "Precision breeding"] Measurement technique Confirm with laboratory Codes LOINC: 92817-1 ICD-10: Z13.79 Clinical summary This test performs whole genome sequencing on bovine samples to identify genetic variants.
TEST-258 Whole Genome Sequencing (10X Technology) Test This test evaluates the entire genome to identify genetic variations, including single nucleotide variants, structural variants, and copy number changes.	Peripheral whole blood or extracted DNA	5 weeks	10,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single-nucleotide variants (SNVs)", "Structural variants (SVs)", "Copy number variations (CNVs)", "Haplotype-resolved digital karyotype"] Parameters [] Preparation [] Indications ["Precision oncology", "Rare disease diagnosis", "Population biobanking", "Strong family history of cancer", "Undiagnosed rare diseases"] Measurement technique Confirm with laboratory Codes LOINC: 83511-7 ICD-10: Z13.71 Clinical summary This test evaluates the entire genome to identify genetic variations, including single nucleotide variants, structural variants, and copy number changes.
TEST-293 Whole Genome Sequencing (30X) & Variant Calling Test This test evaluates the entire human genome to identify genetic variations, including SNVs, indels, CNVs, and structural rearrangements.	Peripheral whole blood (5 mL in EDTA tube)	8 weeks from sample receipt	22,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Copy number variations (CNVs)", "Structural variants", "Mitochondrial variants"] Parameters [] Preparation ["No fasting required.", "Stay well hydrated.", "Inform phlebotomist of anticoagulant or antiplatelet medications."] Indications ["Hereditary cancer predisposition screening", "Rare disease diagnostic workup", "Pharmacogenomic profiling", "Proactive health optimization"] Measurement technique Confirm with laboratory Codes LOINC: 90515-2 ICD-10: Z13.89 Clinical summary This test evaluates the entire human genome to identify genetic variations, including SNVs, indels, CNVs, and structural rearrangements.
TEST-290 Whole Genome Sequencing (30X) with Variant Calling Test This test evaluates the entire genome sequence to identify genetic variants associated with disease risk, cancer predisposition, and drug response.	Peripheral Whole Blood	8 Weeks	30,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Whole genome sequence", "Disease-causing variants", "Cancer predispositions", "Pharmacogenomic markers", "Coding variants", "Non-coding variants", "Structural variants", "CNVs"] Parameters [] Preparation [] Indications ["Assessment of hereditary cancer risk", "Diagnosis of rare genetic diseases", "Pharmacogenomic analysis", "Personalized medicine guidance"] Measurement technique Confirm with laboratory Codes LOINC: 94124-0 ICD-10: Z13.89 Clinical summary This test evaluates the entire genome sequence to identify genetic variants associated with disease risk, cancer predisposition, and drug response.

Category overview

Whole Genome Sequencing: overview

Achieving an absolute, definitive diagnosis for elusive, multi-system disorders requires reading the deepest, most comprehensive layers of your biological code. Representing the pinnacle of our advanced Genomics services, Whole Genome Sequencing (WGS) provides an exhaustive, high-resolution scan of your entire DNA—encompassing both the protein-coding regions and the intricate non-coding sequences that regulate them. Utilizing cutting-edge Next-Generation Sequencing technology, this expansive molecular screening ends the diagnostic odyssey by uncovering extremely rare or novel genetic mutations that all standard and targeted tests miss. This vital genomic data safely guides your healthcare provider in tailoring highly personalized precision medicine, proactive preventative care, and specialized reproductive counseling. Highly regarded for advanced genomic excellence among the best diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, unparalleled analytical accuracy, and incredibly efficient reporting. Secure the ultimate diagnostic insights your health requires—schedule your whole genome sequencing testing in UAE, arrange a secure clinical sample collection, or connect with our specialized medical genetics professionals.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.