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.

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781

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550.00–150,000.00 AED

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Molecular Diagnostics test prices

Showing 391–405 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-874 Human Papillomavirus 16 & 18 (HPV) Viral Load Quantitative Test This test quantifies the amount of HPV DNA from types 16 and 18 in a cervical sample.	Cervical Swab	24 hours (phone) / 3rd working day (email)	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HPV 16 DNA copy number", "HPV 18 DNA copy number"] Parameters [] Preparation ["Avoid intercourse for 48 hours before the test", "Avoid douching for 48 hours before the test", "Avoid vaginal medications/creams/suppositories for 48 hours before the test", "Schedule appointment outside of menstrual period"] Indications ["Risk stratification for cervical precancer", "Monitoring persistent HPV infection", "Guiding colposcopy decisions", "Assessing treatment response"] Measurement technique Confirm with laboratory Codes LOINC: 59262-3 ICD-10: B97.7, Z11.51 Clinical summary This test quantifies the amount of HPV DNA from types 16 and 18 in a cervical sample.
TEST-1496 iAMP21 (Intrachromosomal Amplification of Chromosome 21) FISH Test This diagnostic test evaluates bone marrow aspirate samples for the presence of intrachromosomal amplification of chromosome 21 (iAMP21) using FISH.	Bone Marrow Aspirate	3–4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Intrachromosomal Amplification of Chromosome 21 (iAMP21)", "RUNX1 gene amplification"] Parameters [] Preparation ["No specific patient preparation required, sample collected via bone marrow aspiration by a specialist."] Indications ["Diagnosis and risk stratification of B-cell acute lymphoblastic leukemia (B-ALL)", "Prognostic marker identification in B-ALL"] Measurement technique Confirm with laboratory Codes LOINC: 94373-8 ICD-10: C91.00 Clinical summary This diagnostic test evaluates bone marrow aspirate samples for the presence of intrachromosomal amplification of chromosome 21 (iAMP21) using FISH.
TEST-4816 ICAM1 Gene Test This test identifies genetic variants in the ICAM1 gene associated with an increased risk of developing severe cerebral malaria.	Peripheral Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Variants in the ICAM1 gene", "Genetic susceptibility to cerebral malaria"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Risk stratification for cerebral malaria", "Preventive medicine in malaria-endemic travel zones", "Genetic counseling for at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 91872-4 ICD-10: Z13.79 Clinical summary This test identifies genetic variants in the ICAM1 gene associated with an increased risk of developing severe cerebral malaria.
TEST-4943 ICOS Gene Common Variable Immunodeficiency Type 1 (CVID1) Next‑Generation Sequencing (Genetic Test This genetic test analyzes the ICOS gene for pathogenic variants associated with common variable immunodeficiency type 1 (CVID1). It helps identify the genetic basis for this prima...	Peripheral Whole Blood (3–5 mL in EDTA), or DNA extracted from blood. FTA cards accepted with pre-approval.	3–4 Weeks (expedited options available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ICOS gene", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number alterations"] Parameters [] Preparation ["No special preparation (fasting) is needed."] Indications ["Suspected diagnosis of Common Variable Immunodeficiency Type 1 (CVID1)", "Family history of CVID1", "Guiding immunoglobulin replacement therapy"] Measurement technique Confirm with laboratory Codes LOINC: 101377-5 ICD-10: D83.0 Clinical summary This genetic test analyzes the ICOS gene for pathogenic variants associated with common variable immunodeficiency type 1 (CVID1). It helps identify the genetic basis for this primary immunodeficiency.
TEST-1480 IGHV Mutation Load Test This test evaluates the somatic hypermutation status of the immunoglobulin heavy-chain variable gene (IGHV) in blood or bone marrow samples.	Bone Marrow / Peripheral Blood	7–8 working days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Somatic hypermutation status of IGHV gene", "Prognostic marker for CLL"] Parameters [] Preparation ["Fasting is not required.", "Inform the medical team if you are on anticoagulants or have a bleeding disorder."] Indications ["Diagnosis and prognosis of Chronic Lymphocytic Leukemia (CLL)", "Risk stratification in CLL patients"] Measurement technique Confirm with laboratory Codes LOINC: 98108-3 ICD-10: C91.1 Clinical summary This test evaluates the somatic hypermutation status of the immunoglobulin heavy-chain variable gene (IGHV) in blood or bone marrow samples.
TEST-3346 IGLL1 Gene Agammaglobulinemia Type 2 Autosomal Recessive Genetic Test This genetic test identifies pathogenic variants in the IGLL1 gene, confirming a diagnosis of autosomal recessive agammaglobulinemia type 2.	Whole Blood, Extracted DNA, FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the IGLL1 gene", "Presence of mutations causing agammaglobulinemia type 2"] Parameters [] Preparation ["No specific fasting required", "Inform lab if patient received allogeneic hematopoietic stem cell transplant within 6 months"] Indications ["Suspected primary immunodeficiency", "Diagnosis of autosomal recessive agammaglobulinemia type 2", "Family history of immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 94017-7 ICD-10: D80.0 Clinical summary This genetic test identifies pathogenic variants in the IGLL1 gene, confirming a diagnosis of autosomal recessive agammaglobulinemia type 2.
TEST-1713 IgVH Hypermutation Analysis Confirmatory Test This test evaluates the somatic hypermutation status of the immunoglobulin heavy chain variable gene (IgVH) in peripheral blood.	Peripheral whole blood (lavender-top EDTA tube)	10 working days from sample receipt	3,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Somatic hypermutation status of IgVH gene", "Derived ratio analysis"] Parameters [] Preparation ["No fasting or special preparation required", "Sample collected in a lavender-top EDTA tube"] Indications ["Prognostic stratification in CLL", "Guiding treatment decisions (watch-and-wait vs. early intervention) in CLL"] Measurement technique Confirm with laboratory Codes LOINC: 81264-9 ICD-10: C91.1 Clinical summary This test evaluates the somatic hypermutation status of the immunoglobulin heavy chain variable gene (IgVH) in peripheral blood.
TEST-4706 IL1RN Gene Mutation Analysis (DIRA) Test This test identifies mutations in the IL1RN gene, which cause Deficiency of Interleukin-1 Receptor Antagonist (DIRA).	Whole blood (EDTA) or FTA card	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["IL1RN gene sequence", "Copy Number Variations (CNVs) in IL1RN gene", "Exon-intron boundaries", "5'/3' UTR regions"] Parameters [] Preparation [] Indications ["Suspected Deficiency of Interleukin-1 Receptor Antagonist (DIRA)", "Infants presenting with sterile osteomyelitis and pustular rash", "Family history suggestive of DIRA"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: D89.89 Clinical summary This test identifies mutations in the IL1RN gene, which cause Deficiency of Interleukin-1 Receptor Antagonist (DIRA).
TEST-199 Illumina-Based Bacterial Genome De Novo Assembly and Annotation Test This test evaluates the complete genetic sequence of a bacterial isolate to identify resistance genes, virulence factors, and strain characteristics.	Bacterial isolate (pure culture)	4 weeks	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Whole bacterial genome sequence", "Antibiotic resistance genes", "Virulence factors", "Mobile genetic elements", "Strain-level typing (MLST)", "Plasmid content"] Parameters [] Preparation ["No special preparation needed for blood culture.", "Follow physician's instructions for other specimen types (sputum, urine, swab)."] Indications ["Complex or recurrent infections", "Outbreak investigations", "Suspected antibiotic resistance", "Need for precise pathogen identification", "Epidemiological surveillance"] Measurement technique Confirm with laboratory Codes LOINC: 94061-3 ICD-10: B96.89 Clinical summary This test evaluates the complete genetic sequence of a bacterial isolate to identify resistance genes, virulence factors, and strain characteristics.
TEST-1716 Imatinib Resistance Mutation Analysis (IRMA) Test This test identifies specific mutations within the BCR-ABL kinase domain that confer resistance to imatinib and other TKIs.	Whole Blood (Peripheral)	6 business days from sample receipt	1,100.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCR-ABL kinase domain mutations", "Variant Allele Frequency (VAF)"] Parameters [] Preparation ["No fasting required.", "No specific medication or diet restrictions."] Indications ["Confirmed loss of molecular response to imatinib", "5-10 fold rise in BCR-ABL transcripts", "Progression to accelerated or blast phase disease"] Measurement technique Confirm with laboratory Codes LOINC: 76057-7 ICD-10: C92.10 Clinical summary This test identifies specific mutations within the BCR-ABL kinase domain that confer resistance to imatinib and other TKIs.
TEST-481 Immigration DNA Relationship Test This test confirms or excludes biological relationships (parentage, maternity, siblingship) using forensic DNA genotyping.	Buccal Swab (Oral Mucosa)	10–12 Business Days	3,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Autosomal STR markers", "Y-STR markers"] Parameters [] Preparation ["No fasting required", "Do not discontinue prescribed medications without consulting a doctor"] Indications ["Establishing parentage for visa applications", "Family reunification cases", "Sponsorship applications", "Citizenship applications"] Measurement technique Confirm with laboratory Codes LOINC: 21642-2 ICD-10: Z13.89 Clinical summary This test confirms or excludes biological relationships (parentage, maternity, siblingship) using forensic DNA genotyping.
TEST-3713 Intellectual Disability Panel (NGS) Genetic Test This test identifies pathogenic and likely pathogenic variants in over 600 genes associated with intellectual disability and related neurodevelopmental conditions using Next-Genera...	Peripheral Whole Blood (EDTA)	3–4 weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation [] Indications ["Diagnosis of intellectual disability", "Identification of genetic cause for neurodevelopmental disorders", "Guiding therapeutic and educational interventions", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 93882-9 ICD-10: F70-F79 Clinical summary This test identifies pathogenic and likely pathogenic variants in over 600 genes associated with intellectual disability and related neurodevelopmental conditions using Next-Generation Sequencing.
TEST-2303 Interleukin 28B (IL28B) rs12979860 & rs8099917 Genotyping Test This test evaluates specific genetic variations (SNPs) in the IL28B gene associated with hepatitis C virus (HCV) treatment response and disease progression.	Whole Blood (EDTA)	2–4 Working Days	1,100.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["rs12979860 SNP", "rs8099917 SNP"] Parameters [] Preparation ["No fasting required", "No special diet or medication adjustments needed", "Inform the team of any anticoagulant therapy"] Indications ["Predicting response to interferon-based therapy for Hepatitis C", "Assessing risk of liver disease progression in Hepatitis C"] Measurement technique Confirm with laboratory Codes LOINC: 72517-6 & 72518-4 ICD-10: Z22.52 Clinical summary This test evaluates specific genetic variations (SNPs) in the IL28B gene associated with hepatitis C virus (HCV) treatment response and disease progression.
TEST-2288 Inv(16)(p13q22) / t(16;16)(p13q22) Gene Rearrangement Qualitative PCR Test This test detects the presence or absence of the CBFB-MYH11 gene rearrangement, a specific genetic marker found in certain types of acute myeloid leukemia (AML).	Whole Blood or Bone Marrow Aspirate	Sample Mon/Thu by 11 am → Report Wed/Sat	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CBFB-MYH11 gene rearrangement", "Presence of inv(16)(p13q22) or t(16;16)(p13q22) translocation"] Parameters [] Preparation ["No specific patient preparation required", "Sample collection must be performed in an accredited hospital facility"] Indications ["Diagnosis of AML", "Risk stratification in AML", "Minimal residual disease (MRD) monitoring in AML"] Measurement technique Confirm with laboratory Codes LOINC: 33680-6 ICD-10: C92.8 Clinical summary This test detects the presence or absence of the CBFB-MYH11 gene rearrangement, a specific genetic marker found in certain types of acute myeloid leukemia (AML).
TEST-2320 Inv(16)(p13q22)/t(16;16)(p13;q22) Gene Rearrangement Quantitative MRD Monitoring Test This test quantifies the level of CBFB-MYH11 fusion transcripts in blood or bone marrow to detect minimal residual disease (MRD) in AML patients with the inv(16)/t(16;16) rearrange...	Peripheral blood (10 mL EDTA) or bone marrow (2–3 mL EDTA)	4 Days from sample receipt (samples collected Mon/Thu by 11 am; reports Wed/Sat)	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CBFB-MYH11 fusion transcripts", "Minimal Residual Disease (MRD)"] Parameters [{"name": "MRD Level", "reference_range": " Preparation ["No special preparation required", "Provide completed MRD Requisition Form with historical data"] Indications ["Monitoring AML patients with inv(16)/t(16;16) rearrangement", "Assessing response to therapy", "Detecting early molecular relapse"] Measurement technique Confirm with laboratory Codes LOINC: 69125-5 ICD-10: C92.0 Clinical summary This test quantifies the level of CBFB-MYH11 fusion transcripts in blood or bone marrow to detect minimal residual disease (MRD) in AML patients with the inv(16)/t(16;16) rearrangement.

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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Molecular Diagnostics tests in Dubai & UAE

Molecular Diagnostics test prices

Molecular Diagnostics: overview

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