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Diagnostic options ยท UAE

Genomics tests in Dubai & UAE

Compare available Genomics 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

7

Listed price range

6,000.00โ€“85,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Genomics test prices

Showing 1โ€“7 of 7 matching tests.

Genomics 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
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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
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View 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
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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-173
Polyploid Plant Genome De Novo Assembly and Annotation (Illumina) Test

This test performs de novo assembly and functional annotation of polyploid plant genomes using Illumina sequencing.

Whole blood (2 mL) or extracted genomic DNA (1 ยตg) 8 weeks 85,000.00 AED
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What it measures
["Genome sequence", "Gene locations", "Regulatory elements", "Repetitive regions", "Functional annotations"]
Parameters
[]
Preparation
[]
Indications
["Agricultural research", "Crop improvement studies", "Evolutionary biology studies", "Transcriptomic analysis", "Phenotypic analysis"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 83502-5 ICD-10: Z13.89
Clinical summary
This test performs de novo assembly and functional annotation of polyploid plant genomes using Illumina sequencing.
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
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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
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View 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
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View 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

Genomics: overview

Navigating complex health challenges requires a comprehensive understanding of your entire genetic landscape. The Genomics services at DNA Labs UAE utilize whole-exome and whole-genome sequencing to map the intricate details of your DNA. By evaluating vast genomic data, our advanced genomics testing in the UAE offers unparalleled clarity to assist your physician in developing highly personalized medical strategies. As one of the most trusted diagnostic labs in Dubai/UAE, we handle your sensitive biological data with rigorous confidentiality and provide swift, exceptionally accurate turnaround times. Invest in precision medicine today. Discover our genomics tests, schedule a seamless home sample collection, or reach out to our specialists to begin your analysis.

Before booking

Use the test details as a conversation starter

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.

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