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Diagnostic options Β· UAE

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

550.00–150,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Molecular Diagnostics test prices

Showing 91–105 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-3486
BEST1 Gene Bestrophinopathy Genetic Test

This test evaluates the BEST1 gene for mutations associated with inherited retinal disorders like Best vitelliform macular dystrophy.

Peripheral Blood (Whole Blood EDTA), Dried Blood Spot (FTA card), or Extracted DNA 21–28 business days 2,800.00 AED
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What it measures
["BEST1 gene sequence", "BEST1 gene deletions/duplications"]
Parameters
[]
Preparation
["No specific fasting required", "Avoid recent blood transfusions"]
Indications
["Suspected Best vitelliform macular dystrophy (BVMD)", "Suspected adult-onset vitelliform macular dystrophy (AVMD)", "Family history of bestrophinopathy", "Genetic counselling for inherited retinal disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21655-7 ICD-10: H35.5
Clinical summary
This test evaluates the BEST1 gene for mutations associated with inherited retinal disorders like Best vitelliform macular dystrophy.
TEST-1802
Beta Thalassemia HBB Full Gene Analysis (Single) Test

This test analyzes the entire HBB gene sequence to identify mutations causing beta-thalassemia.

Peripheral Whole Blood 8–10 working days 1,000.00 AED
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What it measures
["Beta-globin gene (HBB) DNA sequence", "Point mutations", "Small deletions", "Splice-site variants"]
Parameters
[]
Preparation
["A doctor’s prescription is required (exemptions apply for surgery, pregnancy, travel)", "No specific fasting or dietary restrictions mentioned"]
Indications
["Diagnosis of beta-thalassemia carrier status", "Diagnosis of beta-thalassemia disease", "Prenatal carrier screening", "Family planning", "Confirmation of inconclusive results from other tests"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21656-4 ICD-10: D56.1
Clinical summary
This test analyzes the entire HBB gene sequence to identify mutations causing beta-thalassemia.
TEST-1806
Beta Thalassemia Test

This test identifies the presence of 12 common mutations in the HBB gene, which are responsible for beta-thalassemia.

Peripheral Whole Blood 6-7 working days 1,200.00 AED
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What it measures
["HBB gene mutations", "Beta-thalassemia carrier status", "Beta-thalassemia disease status"]
Parameters
[]
Preparation
["A washout period of at least 3 months from the last transfusion is required.", "Do not discontinue prescribed medication without consulting your physician."]
Indications
["Carrier screening", "Prenatal diagnosis", "Pre-surgical clearance", "Pregnancy cases", "Travel abroad", "Family history of thalassemia"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 2472-2 ICD-10: D56.1
Clinical summary
This test identifies the presence of 12 common mutations in the HBB gene, which are responsible for beta-thalassemia.
TEST-1004
Beta-Actin Quantitative Test

This diagnostic test evaluates the expression levels of the beta-actin (ACTB) gene, serving as an internal control for molecular assays.

Whole Blood, Culture Cells (cold-chain preserved) 24–36 hours 600.00 AED
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What it measures
["Beta-actin (ACTB) mRNA levels", "Cellular integrity"]
Parameters
[{"name": "Beta-Actin mRNA Levels", "reference_range": null}]
Preparation
["No fasting is needed.", "Bring complete clinical history and a list of all current medications.", "Sign the laboratory consent document provided by the phlebotomist."]
Indications
["Normalization of viral load assays", "Assessment of cellular integrity"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 6211-3 ICD-10: Z01.89
Clinical summary
This diagnostic test evaluates the expression levels of the beta-actin (ACTB) gene, serving as an internal control for molecular assays.
TEST-1005
Beta‑Globin Quantitative Test

This test measures the quantity of beta-globin gene copies in a blood sample.

Peripheral Whole Blood (EDTA) 3rd working day 600.00 AED
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What it measures
["Beta-globin gene copy number", "Beta-globin gene expression level"]
Parameters
[{"name": "Beta-Globin Gene Copy Number", "reference_range": null}]
Preparation
[]
Indications
["Diagnosis of thalassemia syndromes", "Sickle cell disease carrier status identification", "Monitoring gene-therapy responses"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81761-4 ICD-10: D56.1, Z13.79, D56.3
Clinical summary
This test measures the quantity of beta-globin gene copies in a blood sample.
TEST-161
Bisulfite Sequencing Data Analysis (Comprehensive Methylation Profiling) Test

This test evaluates DNA methylation patterns across the entire genome using whole-genome bisulfite sequencing (WGBS). It provides a high-resolution epigenetic snapshot for clinical...

Peripheral whole blood 4 weeks 8,500.00 AED
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What it measures
["DNA methylation marks", "Genome-wide methylation landscapes", "Differentially methylated regions", "Epigenetic age estimate"]
Parameters
[]
Preparation
[]
Indications
["Oncology (cancer risk, tumour characterisation)", "Autoimmune disorders (activity monitoring)", "Epigenetic aging assessment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94082-0 ICD-10: Z01.89
Clinical summary
This test evaluates DNA methylation patterns across the entire genome using whole-genome bisulfite sequencing (WGBS). It provides a high-resolution epigenetic snapshot for clinical insights.
TEST-220
Bisulfite Sequencing Library Preparation for DNA Methylation Analysis Test

This test evaluates DNA methylation patterns across the genome using bisulfite sequencing.

Whole Blood (Peripheral) or Extracted DNA 7 business days 3,000.00 AED
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What it measures
["5-methylcytosine patterns", "Genome-wide methylation"]
Parameters
[]
Preparation
["No fasting or dietary restrictions required.", "Continue usual medications unless advised otherwise by physician.", "Avoid vigorous exercise on the day of collection."]
Indications
["Cancer risk assessment", "Biological aging evaluation", "Gene-regulation dynamics assessment", "Monitoring treatment response"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 83107-8 ICD-10: Z13.89
Clinical summary
This test evaluates DNA methylation patterns across the genome using bisulfite sequencing.
TEST-420
BK Virus Quantitative PCR Test

This test quantifies the amount of BK polyomavirus DNA in a blood plasma or urine sample.

Blood plasma or urine 2–3 working days 900.00 AED
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What it measures
["BK polyomavirus DNA viral load", "Viral replication dynamics"]
Parameters
[{"name": "BK Virus DNA Viral Load", "reference_range": "Varies by laboratory; typically reported as log10 copies/mL. Consult lab report for specific range."}]
Preparation
["No specific fasting required.", "Follow sample collection instructions carefully (clean-catch midstream urine or blood plasma)."]
Indications
["Monitoring kidney transplant recipients", "Detection of BK virus reactivation", "Assessment of risk for BK virus-associated nephropathy (BKVAN)"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 53777-9 ICD-10: B34.8
Clinical summary
This test quantifies the amount of BK polyomavirus DNA in a blood plasma or urine sample.
TEST-6031
BLK Gene Maturity-Onset Diabetes of the Young Type 11 (MODY11) Genetic Test

This test detects pathogenic variants in the BLK gene using Next-Generation Sequencing (NGS). It provides a definitive molecular diagnosis for MODY11.

Peripheral Whole Blood (EDTA) or FTA Card 21–28 Days 2,800.00 AED
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What it measures
["Pathogenic variants in the BLK gene", "Heterozygous mutations"]
Parameters
[]
Preparation
["Fasting is not required", "Pre-test genetic counseling session required"]
Indications
["Suspected MODY11 based on clinical presentation", "Family history of monogenic diabetes", "Need for precise diabetes subtyping for personalized therapy"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 95767-8 ICD-10: E13.8, Z15.89, Z13.1
Clinical summary
This test detects pathogenic variants in the BLK gene using Next-Generation Sequencing (NGS). It provides a definitive molecular diagnosis for MODY11.
TEST-6144
BLM Gene (Bloom Syndrome) Genetic Test

This test analyzes the BLM gene for pathogenic variants associated with Bloom syndrome.

Peripheral whole blood (EDTA tube, 3–5 mL) 3–4 weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the BLM gene"]
Parameters
[]
Preparation
[]
Indications
["Diagnosis of Bloom syndrome", "Assessment of cancer predisposition", "Family cascade testing", "Reproductive planning"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 103225-9 ICD-10: Q82.8
Clinical summary
This test analyzes the BLM gene for pathogenic variants associated with Bloom syndrome.
TEST-997
Bocavirus (RNA Detection) Qualitative Test

This test detects the presence or absence of Human Bocavirus DNA in a patient sample.

Nasopharyngeal Swab / Respiratory Specimen Preliminary verbal result: 36 hours; final verified report: 48 hours. 700.00 AED
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What it measures
["Human Bocavirus DNA"]
Parameters
[]
Preparation
["Avoid natural supplements (e.g., St. John's Wort, high-dose Vitamin C) for 24 hours prior to sampling."]
Indications
["Suspected Bocavirus infection", "Differentiation from other respiratory pathogens", "Antimicrobial stewardship guidance"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 41856-3 ICD-10: B97.89
Clinical summary
This test detects the presence or absence of Human Bocavirus DNA in a patient sample.
TEST-3363
Bone Marrow Failure Anemia Panel Genetic Test

This test evaluates over 145 genes associated with inherited bone marrow failure syndromes using Next-Generation Sequencing.

Peripheral Whole Blood (EDTA Tube) 3–4 Weeks 3,000.00 AED
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What it measures
["Pathogenic germline variants", "Full coding regions and splice-site junctions of 145+ genes"]
Parameters
[]
Preparation
["No fasting required", "Inform laboratory if patient received a blood transfusion within the past 14 days", "Pre-test genetic counseling session is mandatory"]
Indications
["Unexplained cytopenias before age 40", "Family history of bone marrow failure or myelodysplastic syndrome", "Pre-transplant donor screening for familial hematopoietic disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 50398-6 ICD-10: D61.9, D46.9
Clinical summary
This test evaluates over 145 genes associated with inherited bone marrow failure syndromes using Next-Generation Sequencing.
TEST-449
BRAF Mutation Analysis Test

This test identifies somatic BRAF mutations (primarily V600E) in tumour tissue.

Archival Tissue Specimen (FFPE block or slides) 6 Business Days 1,200.00 AED
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What it measures
["BRAF gene mutations", "V600E variant"]
Parameters
[]
Preparation
["No fasting required", "No medication changes required"]
Indications
["Melanoma", "Colorectal carcinoma", "Certain thyroid cancers", "Non-small-cell lung cancers"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94061-7 ICD-10: Z01.818
Clinical summary
This test identifies somatic BRAF mutations (primarily V600E) in tumour tissue.
TEST-1753
BRAF V600E Mutation Analysis Test

This test detects the presence or absence of the BRAF V600E mutation in tumor tissue.

FFPE Tissue Blocks / Biopsy Slides (Archival Specimen) 7–8 working days 1,200.00 AED
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View test specifications and preparation
What it measures
["BRAF V600E mutation"]
Parameters
[]
Preparation
[]
Indications
["Guidance for precision oncology therapy", "Eligibility for BRAF-inhibitor therapy"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 92958-4 ICD-10: Z13.81
Clinical summary
This test detects the presence or absence of the BRAF V600E mutation in tumor tissue.
TEST-6371
BRIP1 Gene Fanconi Anemia Type J Genetic Test

This test evaluates the BRIP1 gene for pathogenic variants associated with Fanconi anemia type J and increased risk of hereditary cancers.

Peripheral Whole Blood (EDTA) or Buccal Swab 3–4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["BRIP1 gene pathogenic variants", "Nucleotide substitutions", "Small insertions/deletions", "Copy number variants"]
Parameters
[]
Preparation
["No fasting required", "Inform phlebotomist about anticoagulants or other medications"]
Indications
["Diagnosis of Fanconi anemia type J", "Assessment of hereditary breast/ovarian cancer risk"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81213-0 ICD-10: D61.0
Clinical summary
This test evaluates the BRIP1 gene for pathogenic variants associated with Fanconi anemia type J and increased risk of hereditary cancers.

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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