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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 481โ€“495 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-1383
Metabolic Disorder Gene Panel Test

This test evaluates genetic variants in over 300 genes associated with inborn errors of metabolism.

Peripheral blood, Amniotic fluid, Chorionic villus sample 4โ€“6 weeks 4,800.00 AED
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What it measures
["Pathogenic variants in metabolic genes", "Copy Number Variations (CNVs)"]
Parameters
[]
Preparation
["Do not discontinue prescribed medication without consulting your doctor"]
Indications
["Diagnosis of suspected inherited metabolic disorder", "Carrier detection", "Personalized management of metabolic conditions"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94306-8 ICD-10: Z13.228
Clinical summary
This test evaluates genetic variants in over 300 genes associated with inborn errors of metabolism.
TEST-5994
Metabolic Disorders NGS Genetic Panel (Wide Range) Test

This test evaluates genetic variations in over 500 genes associated with inborn errors of metabolism.

Whole Blood, Dried Blood Spot (FTA Card), or Extracted DNA 3โ€“4 Weeks 3,000.00 AED
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What it measures
["Genetic variations in metabolic genes", "Presence of mutations linked to metabolic disorders"]
Parameters
[]
Preparation
["No fasting required", "Clinical history review and genetic counseling needed"]
Indications
["Suspected inborn error of metabolism", "Family history of metabolic disorder", "Inconclusive standard metabolic testing"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81407-6 ICD-10: E88.9, E70โ€“E90
Clinical summary
This test evaluates genetic variations in over 500 genes associated with inborn errors of metabolism.
TEST-721
Metapneumovirus B (RNA Detection) Qualitative Test

This test detects the presence of Human Metapneumovirus B RNA in respiratory samples.

Nasopharyngeal swab or sputum 36-48 hours 850.00 AED
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What it measures
["Human Metapneumovirus B RNA"]
Parameters
[]
Preparation
["No fasting required", "Have clinical history ready", "Sign consent form"]
Indications
["Suspected respiratory infection", "Diagnosis of Metapneumovirus B"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 34774-6 ICD-10: B97.81
Clinical summary
This test detects the presence of Human Metapneumovirus B RNA in respiratory samples.
TEST-2531
Methylguanine Methyltransferase (MGMT) Promoter Methylation Test

This diagnostic test evaluates the methylation status of the MGMT gene promoter in tumor tissue.

Fresh biopsy tissue 13 working days (Monday sample receipt) 1,800.00 AED
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What it measures
["Epigenetic silencing of the MGMT gene promoter", "DNA repair capacity related to MGMT"]
Parameters
[]
Preparation
["Submit a fresh biopsy specimen in sterile normal saline.", "Ensure sample is refrigerated and never frozen.", "Completed Genomics Requisition Form 20 must accompany the sample."]
Indications
["Predicting response to alkylating agents (e.g., temozolomide)", "Guiding treatment decisions in glioblastoma and other malignancies", "Determining clinical trial eligibility"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94220-7 ICD-10: C71.9
Clinical summary
This diagnostic test evaluates the methylation status of the MGMT gene promoter in tumor tissue.
TEST-1374
MGMT Methylation Panel Test

This test evaluates the epigenetic silencing of the MGMT gene and methylation metabolites to assess the bodyโ€™s detoxification, DNA repair, and anti-aging capacity.

Peripheral Whole Blood / Archival Tissue (FFPE) 15โ€“20 business days 1,400.00 AED
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What it measures
["MGMT promoter methylation status", "Methylation metabolites", "Key genetic SNPs related to methylation"]
Parameters
[]
Preparation
["No specific fasting required for blood sample.", "Inform phlebotomist of all current medications."]
Indications
["Personalized anti-aging protocols", "Functional medicine assessment", "Evaluation of detoxification pathways", "Assessment of DNA repair capacity"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81132-3 ICD-10: Z13.89
Clinical summary
This test evaluates the epigenetic silencing of the MGMT gene and methylation metabolites to assess the bodyโ€™s detoxification, DNA repair, and anti-aging capacity.
TEST-2539
MI (Molecular Intelligence) Profile Test

This diagnostic test evaluates archival tumor tissue using NGS and IHC to identify actionable genomic alterations and protein expression patterns relevant to cancer treatment.

Archival Tissue Specimen (FFPE Block or Slides) 35 Working Days 65,000.00 AED
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What it measures
["Cancer-related gene mutations (DNA)", "Gene expression levels (RNA)", "Protein expression (IHC)"]
Parameters
[]
Preparation
["No fasting required", "Ensure completed Tumor Profiling Requisition Form (Form 47) and original histopathology report accompany the sample"]
Indications
["Diagnosis of cancer", "Identification of targeted therapy options", "Clinical trial matching", "Personalized oncology treatment planning"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 86247-5 ICD-10: C80.1, Z15.09, Z12.8
Clinical summary
This diagnostic test evaluates archival tumor tissue using NGS and IHC to identify actionable genomic alterations and protein expression patterns relevant to cancer treatment.
TEST-2538
Microsatellite Instability (MSI) by PCR, Fragment Analysis Test

This test evaluates tumor DNA for microsatellite instability, indicating potential defects in DNA mismatch repair.

Formalin-Fixed Paraffin-Embedded (FFPE) Tumor Tissue Block 10 Days 2,000.00 AED
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What it measures
["Microsatellite length variations", "DNA mismatch repair deficiency"]
Parameters
[{"name": "Panel Size", "reference_range": "5-Marker Bethesda Panel + NR-21/NR-24 optional"}, {"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}, {"name": "Diagnostic Specificity", "reference_range": "99.9%"}]
Preparation
[]
Indications
["Eligibility for immune checkpoint inhibitor therapy", "Diagnosis of Lynch syndrome", "Classification of tumors"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81679-5 ICD-10: Z15.09, C18.9, C54.1
Clinical summary
This test evaluates tumor DNA for microsatellite instability, indicating potential defects in DNA mismatch repair.
TEST-48
MiSeq 2ร—250 Paired-End Sequencing Test

This test provides a comprehensive analysis of an individual's DNA sequence using next-generation sequencing technology.

Whole Blood (EDTA) or High-Quality Extracted DNA (โ‰ฅ20 ng/ยตL) 14 days 35,000.00 AED
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What it measures
["DNA sequence variations", "Single nucleotide polymorphisms (SNPs)", "Insertions/Deletions (Indels)", "Copy number variations (CNVs)"]
Parameters
[]
Preparation
["Mandatory pre-test consultation with a DHA-licensed genetic professional.", "Written informed consent required prior to sample collection."]
Indications
["Oncology profiling", "Rare disease gene discovery", "Biobank sample validation", "Diagnosis of inherited genetic disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-9 ICD-10: Z01.818
Clinical summary
This test provides a comprehensive analysis of an individual's DNA sequence using next-generation sequencing technology.
TEST-2020
MITF Gene Melanoma Susceptibility Test

This test evaluates the entire MITF gene for pathogenic variants associated with an increased inherited risk of cutaneous malignant melanoma.

Peripheral Whole Blood (EDTA tube) 3โ€“4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the MITF gene", "Inherited genetic susceptibility to melanoma"]
Parameters
[]
Preparation
["No fasting required", "Provide detailed family history of melanoma or other cancers"]
Indications
["Individuals with a strong family history of melanoma", "Risk stratification for melanoma prevention"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 55233-1 ICD-10: Z31.89
Clinical summary
This test evaluates the entire MITF gene for pathogenic variants associated with an increased inherited risk of cutaneous malignant melanoma.
TEST-179
Mitochondrial Genome Sequencing Analysis Test

This test evaluates the entire mitochondrial genome for pathogenic variants, including SNVs, indels, structural rearrangements, and heteroplasmy levels.

Peripheral Whole Blood 21 โ€“ 28 Business Days 3,000.00 AED
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What it measures
["Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Large structural rearrangements", "Heteroplasmy levels (โ‰ฅ1%)"]
Parameters
[]
Preparation
["No fasting or special preparation is required."]
Indications
["Investigating suspected mitochondrial disorders", "Evaluating oncologic risk associated with mitochondrial dysfunction", "Assessing rheumatologic conditions with unexplained metabolic involvement"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94420-9 ICD-10: Z13.83
Clinical summary
This test evaluates the entire mitochondrial genome for pathogenic variants, including SNVs, indels, structural rearrangements, and heteroplasmy levels.
TEST-1345
MLC1 Gene Mutation Analysis (Agrawal Mutation) Test

This test identifies the specific Agrawal founder mutation in the MLC1 gene, associated with megalencephalic leukoencephalopathy with subcortical cysts (MLC).

Peripheral blood, amniotic fluid, chorionic villi, cord blood 7โ€“8 business days 1,200.00 AED
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What it measures
["MLC1 gene pathogenic variants", "Agrawal founder mutation"]
Parameters
[]
Preparation
[]
Indications
["Confirming diagnosis of MLC", "Carrier screening in families with MLC history", "Prenatal genetic counselling"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-9 ICD-10: G93.89
Clinical summary
This test identifies the specific Agrawal founder mutation in the MLC1 gene, associated with megalencephalic leukoencephalopathy with subcortical cysts (MLC).
TEST-6046
MMAB Gene Methylmalonic Aciduria, cblB Type Genetic Test

This genetic test identifies pathogenic variants in the MMAB gene responsible for methylmalonic aciduria, cblB type.

Peripheral whole blood (EDTA) or FTA card (dried blood spot) 3-4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the MMAB gene", "Copy Number Variants (CNVs) in the MMAB gene"]
Parameters
[]
Preparation
["No specific fasting required", "Inform lab of any recent blood transfusions (within 4 weeks)"]
Indications
["Definitive molecular diagnosis of methylmalonic aciduria, cblB type", "Carrier screening for at-risk family members", "Prenatal planning", "Family risk assessment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81404-6 ICD-10: E71.1
Clinical summary
This genetic test identifies pathogenic variants in the MMAB gene responsible for methylmalonic aciduria, cblB type.
TEST-1976
MMR Genes Methylation Analysis (Genetic Test)

This test evaluates abnormal methylation patterns in DNA mismatch repair genes (MLH1, MSH2, MSH6, PMS2) to help identify Lynch syndrome or sporadic cancers with epigenetic silencin...

Whole Blood, Extracted DNA, or Dried Blood Spot on FTA Card 3โ€“4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Abnormal methylation patterns in MLH1, MSH2, MSH6, PMS2 genes", "Epigenetic silencing of DNA mismatch repair genes"]
Parameters
[]
Preparation
["Do not discontinue prescribed medication without consulting your doctor", "Inform your physician of all current treatments, especially hypomethylating agents or valproic acid"]
Indications
["Diagnosis of Lynch syndrome", "Differentiation of sporadic from hereditary colorectal cancers", "Guiding hereditary cancer surveillance"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-1 ICD-10: Z15.09, Z13.89
Clinical summary
This test evaluates abnormal methylation patterns in DNA mismatch repair genes (MLH1, MSH2, MSH6, PMS2) to help identify Lynch syndrome or sporadic cancers with epigenetic silencing.
TEST-2534
Molecular Intelligence Tumor Seek Test

This test performs comprehensive genomic profiling on FFPE tumor tissue to identify actionable genetic alterations for personalized cancer therapy.

FFPE Tumor Tissue Block (Archival Specimen) 30 Working Days 52,000.00 AED
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What it measures
["DNA mutations", "RNA fusions", "Splice variants", "Gene expression levels", "Over 500 cancer-related genes"]
Parameters
[]
Preparation
[]
Indications
["Patients with solid tumors where targeted therapy is being considered.", "Identification of actionable genetic alterations.", "Guidance for personalized cancer treatment."]
Measurement technique
Confirm with laboratory
Codes
LOINC: 98590-2 ICD-10: C80.1
Clinical summary
This test performs comprehensive genomic profiling on FFPE tumor tissue to identify actionable genetic alterations for personalized cancer therapy.
TEST-1993
MPL Gene Exon 10 NGS Sequencing Test

This test identifies somatic or germline mutations in exon 10 of the MPL gene.

Peripheral Whole Blood (EDTA) or Isolated DNA 3โ€“4 weeks 2,800.00 AED
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What it measures
["MPL gene exon 10 mutations", "Variant Allele Frequency (VAF)"]
Parameters
[]
Preparation
["No fasting required", "Continue all prescribed medications unless advised otherwise by your doctor"]
Indications
["Diagnosis of essential thrombocythemia", "Diagnosis of primary myelofibrosis", "Diagnosis of familial thrombocytosis", "Risk stratification in myeloproliferative neoplasms"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 93111-7 ICD-10: D47.3, D47.1
Clinical summary
This test identifies somatic or germline mutations in exon 10 of the MPL gene.

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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