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Molecular Diagnostics tests in Dubai & UAE

Compare available Molecular Diagnostics 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

781

Listed price range

550.00โ€“150,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

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Molecular Diagnostics test prices

Showing 766โ€“780 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-5522
WFS1 Gene Wolfram Syndrome Type 1 Genetic Test

This genetic test detects pathogenic variants in the WFS1 gene, which are responsible for Wolfram syndrome type 1 (DIDMOAD). It analyzes the complete coding region using next-gener...

Whole Blood, Dried Blood Spot (FTA Card) 3 to 4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the WFS1 gene", "Exonic mutations", "Splice site variants"]
Parameters
[]
Preparation
["No fasting required", "No special diet or medication adjustments needed", "Inform lab of any anticoagulant use", "Pre-test genetic counselling is available and recommended"]
Indications
["Suspected Wolfram syndrome type 1 (DIDMOAD)", "Family history of Wolfram syndrome", "Early onset diabetes mellitus with optic atrophy or hearing loss"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 92765-6 ICD-10: E13.8
Clinical summary
This genetic test detects pathogenic variants in the WFS1 gene, which are responsible for Wolfram syndrome type 1 (DIDMOAD). It analyzes the complete coding region using next-generation sequencing.
TEST-359
Wheat GMO (Genetically Modified Organism) Detection via PCR Test

This test detects and quantifies genetically modified sequences in wheat products using Real-Time PCR.

Dry wheat product (flour, grain, semolina, baked goods) 7 business days 1,000.00 AED
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What it measures
["Presence of genetically modified sequences in wheat"]
Parameters
[]
Preparation
[]
Indications
["Verifying compliance with food safety regulations", "Assessing dietary purity", "Substantiating 'non-GMO' claims"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 48065-3 ICD-10: Z13.9
Clinical summary
This test detects and quantifies genetically modified sequences in wheat products using Real-Time PCR.
TEST-344
Whole Exome + Mitochondrial Genome Sequencing Test

This test evaluates the entire coding region of the genome (exome) and the complete mitochondrial genome to identify genetic variants associated with hereditary disorders, cancer p...

Whole Blood (Peripheral Blood) 3โ€“4 weeks 6,000.00 AED
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What it measures
["Nuclear Exome Variants", "Mitochondrial Genome Variants"]
Parameters
[]
Preparation
["No fasting required", "Inform doctor about recent transfusions or bone marrow transplants"]
Indications
["Complex or undiagnosed conditions", "Hereditary disorders", "Cancer predisposition", "Mitochondrial syndromes"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81237-6 ICD-10: Z01.5, R69
Clinical summary
This test evaluates the entire coding region of the genome (exome) and the complete mitochondrial genome to identify genetic variants associated with hereditary disorders, cancer predisposition, and mitochondrial syndromes.
TEST-558
Whole Exome Sequencing (WES) Test

This test analyzes the protein-coding regions (exome) of the genome to identify genetic variants associated with inherited diseases.

Peripheral whole blood 4 weeks 3,500.00 AED
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What it measures
["Pathogenic variants in protein-coding genes", "Genetic mutations linked to Mendelian disorders"]
Parameters
[]
Preparation
["No special preparation is needed"]
Indications
["Diagnosis of suspected inherited conditions", "Identification of genetic causes for developmental delays", "Evaluation of rare diseases", "Oncogenomics"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-9 ICD-10: Z01.818
Clinical summary
This test analyzes the protein-coding regions (exome) of the genome to identify genetic variants associated with inherited diseases.
TEST-194
Whole Exome Sequencing (WES) with Variant Calling & Annotation Test

This diagnostic test evaluates the protein-coding regions of the genome to identify genetic variants potentially causing inherited disorders.

Peripheral whole blood (EDTA) or extracted gDNA 28 calendar days 3,500.00 AED
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What it measures
["Protein-coding gene variants", "Pathogenic and likely pathogenic variants"]
Parameters
[{"name": "Sequencing Depth", "reference_range": "โ‰ฅ100ร— mean coverage (Illumina platform)"}, {"name": "Variant Calling & Annotation", "reference_range": "GATK-based, ACMG/AMP 5-tier classification, Ensembl VEP"}]
Preparation
[]
Indications
["Individuals with clinical suspicion of a monogenic disorder", "Undiagnosed syndromes", "Developmental delays", "Multiple congenital anomalies", "Inherited neurological disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 93927-4 ICD-10: Z01.81, Z01.89
Clinical summary
This diagnostic test evaluates the protein-coding regions of the genome to identify genetic variants potentially causing inherited disorders.
TEST-2752
Whole Exome Sequencing Trio Test

This test identifies genetic variants in the protein-coding regions of the genome for the proband and both parents to diagnose genetic disorders.

Whole blood (EDTA) 6 Weeks 9,100.00 AED
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What it measures
["Protein-coding regions (exome) of ~20,000 genes", "Variant inheritance patterns", "De novo mutations", "Autosomal recessive disorders", "X-linked conditions"]
Parameters
[]
Preparation
["No specific fasting required", "No specific medication or diet restrictions"]
Indications
["Suspected genetic disorder with unknown cause", "Complex diagnostic odysseys", "Need to differentiate inherited vs. de novo mutations", "Assessment of carrier status in parents"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 93882-7 ICD-10: Z13.79, Z84.81, Z15.89
Clinical summary
This test identifies genetic variants in the protein-coding regions of the genome for the proband and both parents to diagnose genetic disorders.
TEST-185
Whole Genome De Novo Assembly and Annotation (Illumina) Test

This test provides a complete diploid genome map, identifying structural variants, insertions, and regulatory elements.

Peripheral whole blood 8 weeks 32,500.00 AED
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What it measures
["Structural variants", "Novel insertions", "Regulatory elements", "Gene models", "Epigenetic marks"]
Parameters
[]
Preparation
[]
Indications
["Risk stratification for complex diseases", "Personalized preventive strategies", "Discovery of personal pharmacogenomic variants", "Anti-aging interventions"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 83502-8 ICD-10: Z13.89
Clinical summary
This test provides a complete diploid genome map, identifying structural variants, insertions, and regulatory elements.
TEST-180
Whole Genome Sequencing (Diploid Reference, Illumina) Analysis Test

This test evaluates the entire genome to identify genetic variants associated with rheumatologic diseases and aging biomarkers.

Whole Blood (Peripheral Venous) 4 weeks 7,500.00 AED
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What it measures
["Single nucleotide variants (SNVs)", "Structural rearrangements", "Rheumatologic disease pathways", "Aging-associated biomarkers"]
Parameters
[]
Preparation
["Refrain from heavy physical exertion immediately before blood collection."]
Indications
["Investigation of rheumatologic conditions", "Assessment of aging-related genetic factors"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-9 ICD-10: Z13.79
Clinical summary
This test evaluates the entire genome to identify genetic variants associated with rheumatologic diseases and aging biomarkers.
TEST-257
Whole Genome Sequencing (WGS) Test

Whole Genome Sequencing (WGS) analyzes the entire DNA sequence to identify genetic variations associated with health conditions.

Peripheral whole blood 5 weeks 7,500.00 AED
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What it measures
["Pathogenic variants", "Likely pathogenic variants", "Variants of uncertain significance", "Pharmacogenomic markers", "Cancer predisposition syndromes"]
Parameters
[]
Preparation
[]
Indications
["Identification of hereditary disorders", "Pharmacogenomic analysis", "Cancer predisposition assessment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 71822-6 ICD-10: Z13.89
Clinical summary
Whole Genome Sequencing (WGS) analyzes the entire DNA sequence to identify genetic variations associated with health conditions.
TEST-190
Whole Genome Sequencing (WGS) with Vertebrate Reference Genome Analysis Test

This test performs Whole Genome Sequencing (WGS) to analyze germline variants associated with autoimmune and autoinflammatory conditions.

Peripheral whole blood 4 weeks (28 calendar days) from sample receipt 6,500.00 AED
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What it measures
["Germline variants", "Introns", "Regulatory regions", "Deep intronic variants"]
Parameters
[]
Preparation
["Maintain usual fluid intake", "Wear clothing with easy arm access", "No fasting required unless instructed by ordering physician"]
Indications
["Diagnosis of autoimmune and autoinflammatory disorders", "Personalised management plans for these conditions"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 99055-4 ICD-10: Z13.79
Clinical summary
This test performs Whole Genome Sequencing (WGS) to analyze germline variants associated with autoimmune and autoinflammatory conditions.
TEST-291
Whole Genome Sequencing & Variant Calling (10X Genomics) Test

This test evaluates the entire genome for genetic variations, focusing on hereditary cancer syndromes, cardiovascular susceptibility, and pharmacogenomic markers.

Whole blood (peripheral) or pre-extracted DNA 8 weeks (accelerated reporting available) 4,500.00 AED
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What it measures
["Whole Genome Sequence", "Genetic Variants (SNPs, Indels, SVs)", "Haplotypes", "Pharmacogenomic Markers"]
Parameters
[]
Preparation
["No specific fasting required.", "Do not discontinue prescribed medications without consulting a physician."]
Indications
["Assessment of hereditary cancer risk", "Pharmacogenomic analysis for anti-aging", "Investigation of rare diseases", "Cardiovascular risk assessment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 10520-0 ICD-10: Z15.09, Z14.8
Clinical summary
This test evaluates the entire genome for genetic variations, focusing on hereditary cancer syndromes, cardiovascular susceptibility, and pharmacogenomic markers.
TEST-1049
X & Y Chromosome Chimerism Analysis (Sex-Mismatch Bone Marrow Transplant Monitoring) Test

This test evaluates the percentage of donor-derived cells versus recipient-derived cells in blood or bone marrow after a sex-mismatched bone marrow transplant.

Bone Marrow Aspirate or Peripheral Blood 3โ€“4 Days 700.00 AED
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What it measures
["Ratio of donor-derived cells to recipient-derived cells", "Donor engraftment status", "Potential for graft rejection", "Early detection of relapse"]
Parameters
[{"name": "Donor Chimerism Percentage", "reference_range": ">95% (Full Engraftment), 5-95% (Mixed Chimerism),
Preparation
["No specific fasting required", "Continue all prescribed medications unless advised otherwise by your physician"]
Indications
["Post-sex-mismatched bone marrow transplantation monitoring", "Assessment of donor engraftment", "Detection of graft rejection or failure", "Early detection of leukemic relapse"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 96723-7 ICD-10: Z94.84, Z48.22, Z85.6
Clinical summary
This test evaluates the percentage of donor-derived cells versus recipient-derived cells in blood or bone marrow after a sex-mismatched bone marrow transplant.
TEST-1995
XRCC3 Melanoma Susceptibility (Familial Cutaneous Malignant Melanoma Type 6) Genetic Test

This genetic test evaluates for germline mutations within the XRCC3 gene, which are associated with an increased risk of developing familial cutaneous malignant melanoma type 6.

Peripheral Whole Blood 21 to 28 Business Days 2,800.00 AED
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What it measures
["Germline mutations in the XRCC3 gene", "Single nucleotide variants", "Small insertions and deletions", "Splice-site alterations"]
Parameters
[]
Preparation
["No specific fasting required", "Inform clinician of any medications"]
Indications
["Individuals with a personal or family history suggestive of familial cutaneous malignant melanoma type 6", "Risk stratification for melanoma susceptibility"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21636-6 ICD-10: Z15.09
Clinical summary
This genetic test evaluates for germline mutations within the XRCC3 gene, which are associated with an increased risk of developing familial cutaneous malignant melanoma type 6.
TEST-1045
Y Chromosome Microdeletion (16 Mutations) Test

This diagnostic test evaluates for the presence of 16 specific microdeletions within the AZFa, AZFb, and AZFc regions of the Y chromosome.

Peripheral blood (3 mL EDTA) 10 working days 1,000.00 AED
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What it measures
["Y chromosome microdeletions (AZFa, AZFb, AZFc regions)", "Spermatogenic failure genetic markers"]
Parameters
[]
Preparation
["No special preparation needed", "Maintain usual diet and hydration", "No fasting required"]
Indications
["Diagnosis of male infertility", "Evaluation of non-obstructive azoospermia", "Assessment of severe oligozoospermia", "Genetic counseling for male infertility"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 93977-0 ICD-10: Q98.5
Clinical summary
This diagnostic test evaluates for the presence of 16 specific microdeletions within the AZFa, AZFb, and AZFc regions of the Y chromosome.
TEST-3432
Y Chromosome Microdeletion (AZF Region) Genetic Test

This genetic test evaluates the Y chromosome for microdeletions within the AZF regions (AZFa, AZFb, AZFc, AZFd) associated with non-obstructive azoospermia.

Whole Blood (EDTA), FTA Card, or Extracted DNA 3โ€“4 Weeks (from sample receipt at laboratory) 2,800.00 AED
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What it measures
["Y chromosome microdeletions (AZFa, AZFb, AZFc, AZFd)", "Genetic basis of non-obstructive azoospermia"]
Parameters
[]
Preparation
["Do not discontinue prescribed medication, hormonal therapies, antioxidants, or fertility supplements without consulting your infertility specialist."]
Indications
["Diagnosis of non-obstructive azoospermia", "Evaluation before sperm retrieval procedures (e.g., micro-TESE)", "Genetic counseling for male infertility"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94520-7 ICD-10: N46.8, Z31.41, Q98.8, Z14.0
Clinical summary
This genetic test evaluates the Y chromosome for microdeletions within the AZF regions (AZFa, AZFb, AZFc, AZFd) associated with non-obstructive azoospermia.

Category overview

Molecular Diagnostics: overview

When complex health questions arise, evaluating your health at the cellular level provides the definitive clarity necessary for proactive care. At DNA Labs UAE, our Molecular Diagnostics services harness the power of advanced nucleic acid amplification and real-time PCR technologies to detect diseases with unparalleled sensitivity. From identifying viral loads to pinpointing genetic markers, our specialized molecular testing in the UAE gives your healthcare provider the precise data needed to customize your medical strategy. Trust in one of the leading diagnostic labs in Dubai and the UAE to process your samples with rigorous confidentiality and exceptionally fast, accurate turnaround times. Step forward with absolute confidence. View our molecular diagnostics profiles below, request a seamless home sample collection, or contact our specialized team to book your test.

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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.

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