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Diagnostic options ยท 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

550.00โ€“150,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Molecular Diagnostics test prices

Showing 271โ€“285 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-894
Filariasis (RNA Detection) Qualitative Test

This test detects the presence of RNA from specific filarial parasites in the blood, indicating an active infection.

Peripheral Blood (Whole Blood, Serum, or Plasma) 36โ€“48 hours 650.00 AED
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What it measures
["Filarial parasite RNA (Wuchereria bancrofti, Brugia malayi, Brugia timori)", "Active infection status"]
Parameters
[]
Preparation
["No fasting required", "Share complete travel and clinical history with phlebotomist"]
Indications
["Early diagnosis of lymphatic filariasis", "Post-treatment monitoring", "Travel-related screening"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 61796-0 ICD-10: B74.0, B74.1, B74.2, B74.9
Clinical summary
This test detects the presence of RNA from specific filarial parasites in the blood, indicating an active infection.
TEST-349
Finished Feed & Pellets GMO Detection Test

This diagnostic test evaluates finished feed and pellet samples for the presence of specific transgenic DNA sequences commonly used in genetically modified crops.

Finished Feed / Pellet 5 Business Days 1,000.00 AED
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What it measures
["Presence of 35S promoter sequence", "Presence of NOS terminator sequence"]
Parameters
[]
Preparation
[]
Indications
["Regulatory compliance checks", "Feed quality management", "Informed dietary adjustments for livestock"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 48065-7 ICD-10: Z13.9
Clinical summary
This diagnostic test evaluates finished feed and pellet samples for the presence of specific transgenic DNA sequences commonly used in genetically modified crops.
TEST-1134
FIP1L1-PDGFRA Gene Rearrangement Detection Test

This test detects the presence of the FIP1L1-PDGFRA gene fusion, a key marker for specific types of chronic eosinophilic leukemia and hypereosinophilic syndrome.

Whole blood (4 mL, EDTA) or bone marrow aspirate 12 days from sample receipt (Monday 11 AM cutoff) 1,500.00 AED
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What it measures
["FIP1L1-PDGFRA gene fusion", "Presence of specific gene rearrangement"]
Parameters
[]
Preparation
["Inform physician of all medications, especially imatinib or corticosteroids", "Complete Genomics Clinical Information Requisition Form (Form 20)"]
Indications
["Diagnosis of chronic eosinophilic leukemia (CEL)", "Diagnosis of hypereosinophilic syndrome", "Guiding imatinib therapy"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 38288-2 ICD-10: D47.5
Clinical summary
This test detects the presence of the FIP1L1-PDGFRA gene fusion, a key marker for specific types of chronic eosinophilic leukemia and hypereosinophilic syndrome.
TEST-403
Fish Species Authentication Test

This test identifies the specific species of fish present in a sample using DNA FISH technology.

Fresh or frozen fish tissue 14 days 750.00 AED
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What it measures
["Fish species DNA"]
Parameters
[]
Preparation
[]
Indications
["Dietary compliance verification", "Food fraud detection", "Supplement purity confirmation", "Suspected mislabeling"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82910-1 ICD-10: Z01.8
Clinical summary
This test identifies the specific species of fish present in a sample using DNA FISH technology.
TEST-27
FISH-HER2 (ERBB2) Reflex Test

This test determines the amplification status of the HER2 (ERBB2) gene using Fluorescence In Situ Hybridization (FISH) on formalin-fixed paraffin-embedded tissue.

Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block 7 working days 1,500.00 AED
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What it measures
["HER2 (ERBB2) gene copy number", "Chromosome 17 centromere signals"]
Parameters
[]
Preparation
[]
Indications
["Ambiguous HER2 IHC results (2+) in invasive breast cancer", "Guiding targeted anti-HER2 therapy selection"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 32833-0 ICD-10: C50.9
Clinical summary
This test determines the amplification status of the HER2 (ERBB2) gene using Fluorescence In Situ Hybridization (FISH) on formalin-fixed paraffin-embedded tissue.
TEST-4743
FKTN Gene Limb-Girdle Muscular Dystrophy Autosomal Recessive Type 2M (LGMDR2M) Genetic Test

This test analyzes the FKTN gene for pathogenic variants associated with autosomal recessive limb-girdle muscular dystrophy type 2M (LGMDR2M). It uses Next-Generation Sequencing (N...

Whole Blood (EDTA) or Buccal Swab 3โ€“4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the FKTN gene"]
Parameters
[]
Preparation
["No specific fasting required", "Inform phlebotomist of any bleeding disorders or medications"]
Indications
["Suspected diagnosis of Limb-Girdle Muscular Dystrophy Type 2M", "Family history of LGMDR2M", "Carrier screening"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82939-0 ICD-10: G71.0
Clinical summary
This test analyzes the FKTN gene for pathogenic variants associated with autosomal recessive limb-girdle muscular dystrophy type 2M (LGMDR2M). It uses Next-Generation Sequencing (NGS) to detect mutations throughout the gene's coding region.
TEST-4962
FLG Gene Ichthyosis Vulgaris Genetic Test

This test evaluates the entire coding region of the FLG gene to identify pathogenic variants associated with ichthyosis vulgaris.

Whole blood (EDTA tube), extracted DNA, or a single drop of blood on an FTA card 3โ€“4 weeks (expedited 2-week option available for urgent clinical cases) 2,800.00 AED
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What it measures
["FLG gene sequence", "Single nucleotide variants", "Small insertions and deletions", "Copy number alterations"]
Parameters
[]
Preparation
["No fasting or dietary restrictions are needed.", "Continue all prescribed medications unless your doctor specifically instructs otherwise."]
Indications
["Diagnosis of ichthyosis vulgaris", "Cascade testing for at-risk relatives", "Risk stratification for atopic dermatitis"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 86635-0 ICD-10: Q80.0
Clinical summary
This test evaluates the entire coding region of the FLG gene to identify pathogenic variants associated with ichthyosis vulgaris.
TEST-1576
FLT3 (ITD, D835Y) Mutation Detection Test

This test detects the presence of FLT3 internal tandem duplications (ITD) and D835Y point mutations in a patient's leukemia cells.

Peripheral Blood or Bone Marrow Aspirate 3โ€“4 business days 800.00 AED
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What it measures
["FLT3 gene mutations (ITD, D835Y)", "Mutant allele burden"]
Parameters
[{"name": "FLT3 ITD", "reference_range": "Negative"}, {"name": "FLT3 D835Y", "reference_range": "Negative"}]
Preparation
["No specific patient preparation required."]
Indications
["Diagnosis of Acute Myeloid Leukemia (AML)", "Prognosis and risk stratification in AML", "Guidance for targeted therapy selection in AML"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21718-3 ICD-10: C92.0
Clinical summary
This test detects the presence of FLT3 internal tandem duplications (ITD) and D835Y point mutations in a patient's leukemia cells.
TEST-1240
FLT3 Gene Mutation Quantitative Monitoring Test

This test quantifies FLT3 gene mutations (ITD and TKD) in blood or bone marrow to monitor leukemia treatment response and detect relapse.

Peripheral Whole Blood (5 mL EDTA) or Bone Marrow aspirate 48โ€“72 hours post-collection; reports on Wednesday or Saturday 650.00 AED
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What it measures
["FLT3-ITD variant allele frequency", "FLT3 tyrosine kinase domain (TKD) mutations", "Minimal Residual Disease (MRD)"]
Parameters
[{"name": "FLT3-ITD Variant Allele Frequency", "reference_range": "Reported as a percentage (%), typically
Preparation
[]
Indications
["Monitoring response to FLT3 inhibitor therapy in AML", "Assessing minimal residual disease (MRD) in FLT3-mutated AML", "Detecting early relapse in FLT3-mutated AML"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82291-1 ICD-10: C92.62, Z51.81, C92.00
Clinical summary
This test quantifies FLT3 gene mutations (ITD and TKD) in blood or bone marrow to monitor leukemia treatment response and detect relapse.
TEST-1255
FLT3 Gene Mutation Test

This test detects specific mutations (ITD and TKD) in the FLT3 gene, which are important prognostic markers and therapeutic targets in acute myeloid leukemia.

5 mL Whole Blood in EDTA (Lavender Top) or Bone Marrow Aspirate 7 Days (1 Week) 700.00 AED
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What it measures
["FLT3-ITD mutations", "FLT3-TKD mutations"]
Parameters
[]
Preparation
["No fasting required."]
Indications
["Diagnosis of acute myeloid leukemia (AML)", "Risk stratification in AML", "Guidance for targeted therapy selection in AML"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 49956-1 ICD-10: C92.00
Clinical summary
This test detects specific mutations (ITD and TKD) in the FLT3 gene, which are important prognostic markers and therapeutic targets in acute myeloid leukemia.
TEST-1582
FLT3/ITD Allelic Ratio Test

This test quantifies the ratio of mutated to wild-type FLT3 alleles, providing crucial prognostic information for AML patients.

Bone marrow or peripheral blood 8โ€“10 working days 1,000.00 AED
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What it measures
["FLT3/ITD Allelic Ratio", "Internal Tandem Duplications (ITD)"]
Parameters
[]
Preparation
[]
Indications
["Risk stratification in Acute Myeloid Leukemia (AML)", "Prognosis determination in AML", "Targeted therapy selection for FLT3 inhibitors"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 92806-8 ICD-10: C92.00
Clinical summary
This test quantifies the ratio of mutated to wild-type FLT3 alleles, providing crucial prognostic information for AML patients.
TEST-2942
FOXH1 Gene Test

This test detects pathogenic variants in the FOXH1 gene associated with congenital heart disease and transposition of the great arteries.

Whole Blood (EDTA), Extracted DNA, or FTA Card 3โ€“4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the FOXH1 gene", "Single nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variants (CNVs)"]
Parameters
[]
Preparation
[]
Indications
["Neonatal and paediatric patients with suspected congenital heart disease", "Patients with suspected transposition of the great arteries", "Family screening for CHD"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 103206-3 ICD-10: Q20.3, Q24.9
Clinical summary
This test detects pathogenic variants in the FOXH1 gene associated with congenital heart disease and transposition of the great arteries.
TEST-4709
FOXRED1 Gene Test

This test analyzes the FOXRED1 gene to detect pathogenic variants associated with autosomal recessive Leigh syndrome.

Peripheral Whole Blood (3โ€“5 mL in EDTA tube) or Extracted DNA 3โ€“4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the FOXRED1 gene", "Single-nucleotide variants", "Small insertions or deletions"]
Parameters
[]
Preparation
["No specific fasting required.", "Inform the lab of any medications being taken."]
Indications
["Suspected Leigh syndrome", "Family history of Leigh syndrome", "Progressive neurometabolic disorder"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81262-6 ICD-10: E88.81
Clinical summary
This test analyzes the FOXRED1 gene to detect pathogenic variants associated with autosomal recessive Leigh syndrome.
TEST-1256
Fragile X (FMR1) Carrier Test

This test evaluates the number of CGG repeats in the FMR1 gene to determine carrier status for Fragile X syndrome.

Whole Blood (EDTA tube) 12โ€“15 business days 1,800.00 AED
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What it measures
["CGG repeat expansions in the FMR1 gene"]
Parameters
[]
Preparation
["Do not discontinue prescribed medication without consulting your doctor.", "Inform your physician about all medications and supplements."]
Indications
["Family history of Fragile X syndrome", "Preconception screening", "Informed reproductive planning"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21780-5 ICD-10: Z13.71
Clinical summary
This test evaluates the number of CGG repeats in the FMR1 gene to determine carrier status for Fragile X syndrome.
TEST-188
Fungal Genome De Novo Assembly and Annotation (Illumina) Test

This test identifies the specific fungal species, virulence factors, and antifungal resistance genes present in a sample.

Whole blood (EDTA) or purified fungal culture 4 weeks (28 calendar days) 3,000.00 AED
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What it measures
["Fungal species identification", "Virulence factors", "Antifungal resistance genes (e.g., ERG11, FKS1)"]
Parameters
[]
Preparation
["No fasting or special preparation required", "Inform doctor about all antifungal medications being taken"]
Indications
["Recurrent, invasive, or antifungal-resistant infections", "Failure of conventional culture and sensitivity testing", "Epidemiological typing", "Clinical research"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82147-2 ICD-10: B49
Clinical summary
This test identifies the specific fungal species, virulence factors, and antifungal resistance genes present in a sample.

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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