Next Generation Sequencing tests in Dubai & UAE

Compare available Next Generation Sequencing 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

Listed price range

2,800.00–55,000.00 AED

Clinical preparation

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Next Generation Sequencing test prices

Showing 1–5 of 5 matching tests.

Next Generation Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
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	View
View test specifications and preparation Hide test specifications and preparation 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 (≥20 ng/µL, A260/A280 1.8–2.0)"}] Preparation ["Provide extracted DNA (≥20 ng/µL, A260/A280 1.8–2.0)", "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-3580 AIPL1 Gene Cone-Rod Dystrophy Genetic Testing (NGS) Test This test evaluates the AIPL1 gene for pathogenic variants associated with cone-rod dystrophy using Next-Generation Sequencing (NGS). It identifies mutations linked to progressive...	Peripheral whole blood	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 AIPL1 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation [] Indications ["Diagnosis of inherited cone-rod dystrophy", "Carrier status determination", "Family planning and recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 91831-1 ICD-10: H35.54 Clinical summary This test evaluates the AIPL1 gene for pathogenic variants associated with cone-rod dystrophy using Next-Generation Sequencing (NGS). It identifies mutations linked to progressive vision loss.
TEST-215 ddRAD (Double Digest Restriction Site Associated DNA) Library Preparation Service Test This test constructs reduced-representation DNA libraries for genomic analysis.	Peripheral Whole Blood (2–4 mL in EDTA) or Extracted DNA	1 Week	20,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single Nucleotide Polymorphisms (SNPs)", "Genotyping data"] Parameters [] Preparation [] Indications ["Population genetics studies", "Cancer susceptibility research", "Pharmacogenomics research", "SNP discovery"] Measurement technique Confirm with laboratory Codes LOINC: 93584-1 ICD-10: Z13.89 Clinical summary This test constructs reduced-representation DNA libraries for genomic analysis.
TEST-275 ddRAD Sequencing and Primary Analysis (96 Samples) Test This test identifies genetic variants in targeted regions relevant to cancer predisposition and autoimmune diseases.	Whole Blood (EDTA tube, 4 mL) or Extracted DNA (≥200 ng, TE buffer)	8 weeks (from sample receipt to report delivery)	55,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Insertions and deletions (indels)", "Copy number alterations (CNAs)", "Pathogenic mutations in cancer predisposition genes", "Genetic markers in autoimmune diseases"] Parameters [] Preparation ["No special dietary or medication preparation required.", "Inform phlebotomist about anticoagulant medications.", "Notify lab if recent blood transfusion or bone marrow transplant (within 3 months)."] Indications ["Cancer predisposition risk assessment", "Targeted therapy selection in oncology", "Genetic marker identification in autoimmune/autoinflammatory diseases"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Z13.89 Clinical summary This test identifies genetic variants in targeted regions relevant to cancer predisposition and autoimmune diseases.
TEST-190 Whole Genome Sequencing (WGS) with Vertebrate Reference Genome Analysis Test This test performs Whole Genome Sequencing (WGS) to analyze germline variants associated with autoimmune and autoinflammatory conditions.	Peripheral whole blood	4 weeks (28 calendar days) from sample receipt	6,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Germline variants", "Introns", "Regulatory regions", "Deep intronic variants"] Parameters [] Preparation ["Maintain usual fluid intake", "Wear clothing with easy arm access", "No fasting required unless instructed by ordering physician"] Indications ["Diagnosis of autoimmune and autoinflammatory disorders", "Personalised management plans for these conditions"] Measurement technique Confirm with laboratory Codes LOINC: 99055-4 ICD-10: Z13.79 Clinical summary This test performs Whole Genome Sequencing (WGS) to analyze germline variants associated with autoimmune and autoinflammatory conditions.

Category overview

Next Generation Sequencing: overview

Resolving complex medical mysteries requires the most advanced technology available, offering you clear, comprehensive answers for ultimate peace of mind. Central to our Molecular Diagnostics division, our Next Generation Sequencing (NGS) services allow for rapid, simultaneous analysis of millions of DNA strands. This unparalleled depth of next generation sequencing data acts as a powerful tool for your physician, delivering the molecular clarity required for highly personalized medical guidance rather than an isolated clinical diagnosis. Renowned among top diagnostic labs in Dubai and the UAE, DNA Labs UAE guarantees rigorous patient privacy alongside exceptionally fast, precise turnaround times. Harness the power of modern genomics today: review our next generation sequencing testing in the UAE below to book an appointment, schedule a seamless home collection, or speak with our dedicated specialists.

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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.