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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 1โ€“15 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-2179 Featured
Breast Cancer BRCA1 & BRCA2 Gene Test

This diagnostic test evaluates the full coding regions of the BRCA1 and BRCA2 genes for inherited pathogenic variants associated with hereditary cancer syndromes.

Blood EDTA tube 3 weeks 1,800.00 AED
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What it measures
["Pathogenic variants in BRCA1 gene", "Pathogenic variants in BRCA2 gene", "Point mutations", "Small insertions/deletions", "Copy number variants (CNVs)"]
Parameters
[]
Preparation
[]
Indications
["Personal or family history of breast cancer", "Personal or family history of ovarian cancer", "Personal or family history of prostate cancer", "Personal or family history of pancreatic cancer", "Assessment of hereditary cancer risk"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94215-7 ICD-10: Z15.01
Clinical summary
This diagnostic test evaluates the full coding regions of the BRCA1 and BRCA2 genes for inherited pathogenic variants associated with hereditary cancer syndromes.
TEST-1031 Featured
Genealogy Family Tree Ancestry DNA Test

This test evaluates ancestry-informative markers across autosomal, mitochondrial, and Y-chromosome DNA to determine ethnic origins and lineage.

Buccal Swab / Saliva 7โ€“10 Business Days 1,500.00 AED
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What it measures
["Autosomal DNA markers", "Mitochondrial DNA (mtDNA) haplogroups", "Y-chromosome DNA (Y-DNA) haplogroups", "Ancestry-informative markers"]
Parameters
[]
Preparation
[]
Indications
["Personal heritage discovery", "Genealogical research", "Anthropological tracing"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-9 ICD-10: Z13.89
Clinical summary
This test evaluates ancestry-informative markers across autosomal, mitochondrial, and Y-chromosome DNA to determine ethnic origins and lineage.
TEST-525 Featured
Paternity DNA Test

This test determines the probability of paternity by comparing genetic markers between a child and an alleged father.

Buccal Swab or Peripheral Blood (standard); Hair, Nails, Toothbrush, Earwax (forensic non-standard) 5 Working Days 1,500.00 AED
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What it measures
["Short Tandem Repeats (STR) at 28 loci", "Combined Paternity Index (CPI)"]
Parameters
[]
Preparation
[]
Indications
["Establishing biological parentage for personal knowledge"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 35290-8 ICD-10: Z02.81
Clinical summary
This test determines the probability of paternity by comparing genetic markers between a child and an alleged father.
TEST-555 Featured
Sibling DNA Test

This test evaluates the genetic relationship between two individuals to determine the probability of them being full, half, or unrelated siblings.

Buccal swab (oral epithelial cells) or venous whole blood 10 business days 3,000.00 AED
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What it measures
["Autosomal Short Tandem Repeats (STRs)", "Likelihood Ratio Calculation"]
Parameters
[]
Preparation
["Bring valid Emirates ID or passport for each participant.", "Sign the informed consent form before sample collection."]
Indications
["Establishing paternity/maternity", "Legal proceedings", "Immigration purposes", "Personal confirmation of relationship"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21642-5 ICD-10: Z02.89
Clinical summary
This test evaluates the genetic relationship between two individuals to determine the probability of them being full, half, or unrelated siblings.
TEST-15 Featured
Whole Exome Sequencing (Exome Max) Test

This test evaluates the DNA sequence of protein-coding regions across the entire exome to identify genetic variants.

Peripheral Whole Blood (5ml) 4 weeks 3,000.00 AED
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What it measures
["Pathogenic variants in ~20,000 protein-coding genes", "Pharmacogenomic markers", "Hereditary cancer syndromes", "Single-gene disorders"]
Parameters
[]
Preparation
["No specific fasting required", "Inform phlebotomist of any medications"]
Indications
["Diagnosis of rare genetic disorders", "Hereditary cancer risk assessment", "Pharmacogenomic analysis", "Personalized preventive medicine"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 62374-9 ICD-10: Z01.89
Clinical summary
This test evaluates the DNA sequence of protein-coding regions across the entire exome to identify genetic variants.
TEST-226
12 Kb Mate-Pair Library Preparation (NGS) Test

This test evaluates the genome for large-scale structural variations, including deletions, duplications, inversions, and translocations.

Whole Blood (EDTA) โ€“ 10 mL or High Molecular Weight DNA (โ‰ฅ5 ยตg) 12 working days 12,500.00 AED
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What it measures
["Structural Variants", "Copy Number Variations", "Genomic Rearrangements"]
Parameters
[]
Preparation
["No special fasting required", "Continue all prescribed medications", "Inform phlebotomist of any anticoagulants"]
Indications
["Detection of structural variants", "Diagnosis of complex genetic disorders", "Research applications requiring large-insert libraries"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 48509-0 ICD-10: Z01.81
Clinical summary
This test evaluates the genome for large-scale structural variations, including deletions, duplications, inversions, and translocations.
TEST-41
2 x 150 HiSeq Sequencing Test

This test evaluates specific genomic regions using high-resolution sequencing to identify potential predispositions and provide insights for personalized health strategies.

High-purity extracted DNA or Whole blood 4 weeks 1,200.00 AED
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What it measures
["Coding regions", "Clinically relevant non-coding regions"]
Parameters
[]
Preparation
["No special preparation is required."]
Indications
["Oncology predisposition screening", "Anti-aging medicine", "Advanced genomic research applications"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 62374-4 ICD-10: Z01.8
Clinical summary
This test evaluates specific genomic regions using high-resolution sequencing to identify potential predispositions and provide insights for personalized health strategies.
TEST-32
2x150 HiSeq Sequencing (20 GB) Test

This test performs whole-genome sequencing to identify genetic variations.

Whole Blood (Peripheral) or Buccal Swab 4 weeks 6,500.00 AED
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What it measures
["Single nucleotide variants", "Copy number changes", "Structural rearrangements"]
Parameters
[]
Preparation
[]
Indications
["Oncology biomarker discovery", "Rare disease research", "Population genomics"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81244-0 ICD-10: Z01.818
Clinical summary
This test performs whole-genome sequencing to identify genetic variations.
TEST-43
2x300 MiSeq Sequencing Flow Cell Test

This test performs ultra-deep paired-end next-generation sequencing to detect genetic variants.

Extracted DNA 14 working days (guaranteed) 45,000.00 AED
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What it measures
["Single nucleotide variants", "Small insertions/deletions", "Structural variants"]
Parameters
[{"name": "Sequencing Platform", "reference_range": "Illumina MiSeq (2x300 bp paired-end)"}, {"name": "Quality Scores", "reference_range": "Q30 > 85% (base accuracy > 99.9%)"}, {"name": "Sample Type", "reference_range": "Extracted DNA (โ‰ฅ20 ng/ยตL, A260/A280 1.8โ€“2.0)"}]
Preparation
["Provide extracted DNA (โ‰ฅ20 ng/ยตL, A260/A280 1.8โ€“2.0)", "Ship sample in ISO-certified cold-chain kit"]
Indications
["Oncology", "Rare disease research", "Pharmacogenomics", "Anti-aging studies"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 60289-1 ICD-10: Z01.818
Clinical summary
This test performs ultra-deep paired-end next-generation sequencing to detect genetic variants.
TEST-230
3kb Mate-Pair Library Preparation Test

This test detects large structural variants (deletions, duplications, inversions, translocations) down to 3kb resolution using long-insert sequencing and Hi-C.

Whole blood (peripheral blood) or high-molecular-weight DNA 12 calendar days 6,000.00 AED
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What it measures
["Structural Variants (SVs)", "Genomic Rearrangements"]
Parameters
[]
Preparation
[]
Indications
["Suspicion of large genomic rearrangements >3kb", "Research applications in ageing and mosaicism"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 51966-0 ICD-10: Z13.71, Z13.89
Clinical summary
This test detects large structural variants (deletions, duplications, inversions, translocations) down to 3kb resolution using long-insert sequencing and Hi-C.
TEST-223
7 Kb Matepair Library Preparation Test

This test evaluates the genome for large structural variations using long-insert sequencing.

Whole Blood (Peripheral) 12 Days 10,000.00 AED
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What it measures
["Structural variants", "Copy-number variations (CNVs)", "Complex chromosomal rearrangements"]
Parameters
[]
Preparation
[]
Indications
["Detection of structural variants >5 kb", "Diagnosis of complex genetic disorders", "Investigation of unexplained developmental delays or congenital anomalies"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81253-9 ICD-10: Z13.89
Clinical summary
This test evaluates the genome for large structural variations using long-insert sequencing.
TEST-385
A1/A2 Milk Testing Test

This test identifies the specific beta-casein allele (A1 or A2) present in a milk sample.

Milk (bovine) โ€“ fresh or commercially packaged 1 week 600.00 AED
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What it measures
["Beta-casein protein variant (A1 or A2)", "Single-nucleotide polymorphism (SNP) discrimination"]
Parameters
[]
Preparation
["No fasting required", "No specific medication or diet restrictions"]
Indications
["Individuals experiencing potential A1 milk sensitivity", "Dietary guidance for digestive comfort related to milk consumption"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94406-7 ICD-10: Z13.89
Clinical summary
This test identifies the specific beta-casein allele (A1 or A2) present in a milk sample.
TEST-3598
ABCA4 Gene Cone-Rod Dystrophy Type 3 Genetic Test

This test identifies pathogenic variants in the ABCA4 gene associated with Cone-Rod Dystrophy Type 3.

Peripheral Whole Blood (3-5 ml EDTA) or Saliva (Oragene DNA Kit) 3 to 4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in ABCA4 gene", "Copy Number Variations (CNV) in ABCA4 gene", "Deep intronic variants in ABCA4 gene"]
Parameters
[]
Preparation
["No specific fasting required", "Do not discontinue prescribed medications unless advised by your physician"]
Indications
["Diagnosis of Cone-Rod Dystrophy Type 3", "Carrier screening for ABCA4-related disorders", "Prognostic information for affected individuals", "Family planning guidance"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 48006-5 ICD-10: H35.54, Z13.5, Z14.8
Clinical summary
This test identifies pathogenic variants in the ABCA4 gene associated with Cone-Rod Dystrophy Type 3.
TEST-6103
ABCB11 Gene Progressive Intrahepatic Cholestasis Type 2 (PFIC2) Genetic Test

This test evaluates the ABCB11 gene for mutations associated with Progressive Familial Intrahepatic Cholestasis Type 2 (PFIC2). It uses Next-Generation Sequencing (NGS) for compreh...

Peripheral Whole Blood 3โ€“4 Weeks 2,800.00 AED
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What it measures
["ABCB11 gene mutations", "Genetic variants associated with PFIC2"]
Parameters
[]
Preparation
["Mandatory pre-test genetic counselling session", "Pedigree chart required"]
Indications
["Diagnosis of PFIC2", "Familial risk assessment", "Guiding targeted therapy", "Pre-transplant evaluation"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21629-5 ICD-10: K76.8
Clinical summary
This test evaluates the ABCB11 gene for mutations associated with Progressive Familial Intrahepatic Cholestasis Type 2 (PFIC2). It uses Next-Generation Sequencing (NGS) for comprehensive analysis.
TEST-6329
ABCC8 Gene Permanent Neonatal Diabetes Mellitus Genetic Test

This genetic test analyzes the ABCC8 gene to detect pathogenic variants associated with permanent neonatal diabetes mellitus.

Whole Blood (EDTA tube) or Buccal Swab 3-4 Weeks 2,800.00 AED
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What it measures
["ABCC8 gene variants", "Pathogenic mutations"]
Parameters
[]
Preparation
["No special preparation required", "Ensure clinical history form and signed consent are ready"]
Indications
["Diagnosis of permanent neonatal diabetes mellitus", "Identification of ABCC8 gene mutations"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94708-3 ICD-10: P70.2
Clinical summary
This genetic test analyzes the ABCC8 gene to detect pathogenic variants associated with permanent neonatal diabetes mellitus.

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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