Diagnostic options · UAE

Sequencing tests in Dubai & UAE

Compare available 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

750.00–50,000.00 AED

Clinical preparation

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Sequencing test prices

Showing 16–19 of 19 matching tests.

Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-251 Mitochondrial Genome Sequencing (mtDNA Full‑Sequence) Test This test analyzes the entire mitochondrial DNA sequence to identify pathogenic variants and heteroplasmy levels.	Whole blood (peripheral) or extracted DNA	5 weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single-nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Heteroplasmy levels (down to 1%)"] Parameters [] Preparation ["No special preparation such as fasting is required.", "Inform phlebotomist if taking anticoagulant medications."] Indications ["Evaluation of suspected mitochondrial disorders (MELAS, MERRF, Leigh syndrome, LHON)", "Assessment of mitochondrial dysfunction in oncology", "Investigation of unexplained neurological or metabolic symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 92630-0 ICD-10: E88.49 Clinical summary This test analyzes the entire mitochondrial DNA sequence to identify pathogenic variants and heteroplasmy levels.
TEST-29 PacBio Sequel II 1GB Long-Read Sequencing (HiFi) Test This test evaluates the entire genome using long-read sequencing to identify large-scale genetic variations and structural rearrangements.	Whole blood (2-5 mL EDTA) or high-quality extracted DNA (≥50 ng/µL, OD 260/280 1.8-2.0)	4 weeks	9,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Structural variants", "Repeat expansions", "Pseudo-gene regions", "Haplotype-resolved data", "Whole genome sequence"] Parameters [{"name": "Accuracy", "reference_range": ">99% consensus accuracy (HiFi reads)"}, {"name": "Quality", "reference_range": "Q30 quality"}, {"name": "Throughput", "reference_range": "1GB"}, {"name": "DNA Concentration", "reference_range": "≥ 50 ng/µL"}, {"name": "OD 260/280 Ratio", "reference_range": "1.8-2.0"}] Preparation ["No specific fasting required.", "Do not discontinue prescribed medication without consulting your physician."] Indications ["Detection of large structural variants", "Investigation of repeat expansion disorders", "De novo assembly", "Phasing studies", "Complex genetic investigations"] Measurement technique Confirm with laboratory Codes LOINC: 81248-8 ICD-10: Z13.89 Clinical summary This test evaluates the entire genome using long-read sequencing to identify large-scale genetic variations and structural rearrangements.
TEST-5816 SERHL2 Gene Serine Hydrolase Deficiency, SERHL2-Related Genetic Test This test identifies pathogenic variants in the SERHL2 gene associated with serine hydrolase deficiency.	Peripheral whole blood (EDTA tube) or FTA card (dried blood spot)	3 to 4 Weeks (21–28 Days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SERHL2 gene"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting your doctor"] Indications ["Patients with unexplained metabolic crises", "Patients with muscle weakness", "Patients with neurological decline", "Patients presenting with recurrent metabolic acidosis", "Patients presenting with myopathy", "Patients presenting with developmental regression"] Measurement technique Confirm with laboratory Codes LOINC: 94244-9 ICD-10: E70.8 Clinical summary This test identifies pathogenic variants in the SERHL2 gene associated with serine hydrolase deficiency.
TEST-176 Vertebrate Genome De Novo Assembly and Annotation (Illumina) Test This test performs de novo assembly and annotation of a vertebrate genome using Illumina sequencing.	Peripheral whole blood	8 weeks	45,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Complete genome sequence", "Structural and functional annotation"] Parameters [] Preparation ["Avoid anticoagulants 48 hours before blood draw", "Avoid antiplatelet agents 48 hours before blood draw", "Avoid high-dose fish oil 48 hours before blood draw"] Indications ["Rare disease research", "Pharmacogenomics", "Conservation genomics"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Z13.89 Clinical summary This test performs de novo assembly and annotation of a vertebrate genome using Illumina sequencing.

Category overview

Sequencing: overview

Achieving a definitive diagnosis for complex, multi-system symptoms requires the most comprehensive look at your fundamental biological blueprint to unlock the truth. As a cornerstone of our advanced Genetics services, DNA Sequencing provides an incredibly detailed, high-resolution reading of your genetic code. Utilizing cutting-edge diagnostic technology, this expansive molecular screening helps uncover rare genetic variants and structural changes that standard tests miss, safely guiding your healthcare provider in tailoring highly personalized medical treatments. Recognized as a premier destination for advanced molecular care among diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, uncompromising diagnostic accuracy, and rapid reporting. Take control of your personalized healthcare journey—book your sequencing testing in UAE, arrange a secure home sample collection, or consult our dedicated medical genetics experts today.

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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.