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

2,000.00–30,000.00 AED

Clinical preparation

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Next-Generation Sequencing test prices

Showing 1–7 of 7 matching tests.

Next-Generation Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-45 2x150 HiSeq Sequencing (Single Lane) Test This test provides a comprehensive analysis of the entire genome using high-throughput sequencing technology.	Whole Blood (EDTA) or Extracted DNA	3 weeks (standard); 10 to 14 business days (expedited)	25,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants", "Insertions", "Deletions", "Copy number alterations", "Structural rearrangements", "Whole genome coverage"] Parameters [] Preparation ["Fasting is not required"] Indications ["Oncogenomic profiling", "Inherited disease screening", "Pharmacogenomics", "Anti-aging research"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Z13.71 Clinical summary This test provides a comprehensive analysis of the entire genome using high-throughput sequencing technology.
TEST-99 Eukaryotic mRNA Sequencing Test This test evaluates the complete transcriptome using ultra-low input RNA to identify gene expression patterns, fusions, and splicing variations.	Whole blood (PAXgene/Tempus RNA Tube) or Purified total RNA (10 pg – 1 ng)	5 weeks	3,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Gene expression levels", "Gene fusions", "Alternative splicing events", "Transcriptome profile"] Parameters [] Preparation ["Stop heparin for 48 hours before collection", "Inform phlebotomist about all medications", "Collect blood in PAXgene or Tempus RNA Tube"] Indications ["Detection of gene fusions", "Analysis of alternative splicing", "Characterization of expression signatures", "Investigation of rare or precious samples", "Liquid biopsies", "Circulating tumor cells"] Measurement technique Confirm with laboratory Codes LOINC: 44702-4 ICD-10: Z01.89 Clinical summary This test evaluates the complete transcriptome using ultra-low input RNA to identify gene expression patterns, fusions, and splicing variations.
TEST-37 HiSeq 2x150 Sequencing (10 GB Data) Test This test performs high-throughput next-generation sequencing to generate comprehensive genomic data.	Whole blood (5 mL EDTA) or extracted DNA	4 weeks	3,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants", "Insertions/deletions", "Copy number changes", "Genomic data (Whole Genome or Targeted Resequencing)"] Parameters [] Preparation [] Indications ["Oncology", "Precision anti-ageing programmes", "Research applications"] Measurement technique Confirm with laboratory Codes LOINC: 91806-7 ICD-10: Z13.89 Clinical summary This test performs high-throughput next-generation sequencing to generate comprehensive genomic data.
TEST-35 HiSeq NGS 2×150 bp Sequencing Test This test provides a comprehensive genomic dataset using next-generation sequencing to identify genetic variations.	Whole blood (peripheral)	4 weeks	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genomic DNA sequence variations", "Paired-end 150 bp reads"] Parameters [{"name": "Data Output", "reference_range": "5 GB FASTQ file"}, {"name": "Sequencing Platform", "reference_range": "Illumina HiSeq"}, {"name": "Read Length", "reference_range": "2×150 bp paired-end"}, {"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}] Preparation ["No specific fasting required", "No medication or diet restrictions unless advised by physician"] Indications ["Investigation of hereditary cancer syndromes (e.g., BRCA1/2, Lynch)", "Diagnosis of rare undiagnosed diseases", "Pharmacogenomic profiling", "Research purposes"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Z13.89 Clinical summary This test provides a comprehensive genomic dataset using next-generation sequencing to identify genetic variations.
TEST-47 MiSeq 2x150 bp Paired‑End Sequencing (Flow Cell) Test This test provides a comprehensive genetic profile by sequencing DNA fragments from both ends.	Extracted DNA or Whole Blood (EDTA)	2 weeks	30,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genetic variants", "Somatic mutations", "Anti-aging risk factors"] Parameters [] Preparation ["No special fasting required"] Indications ["Oncology profiling", "Anti-aging risk stratification", "Advanced biomedical research"] Measurement technique Confirm with laboratory Codes LOINC: 92822-6 ICD-10: Z01.81 Clinical summary This test provides a comprehensive genetic profile by sequencing DNA fragments from both ends.
TEST-5041 MYO5A Gene (Griscelli Syndrome Type 1) Genetic Test This test evaluates the MYO5A gene for mutations associated with Griscelli syndrome type 1.	Peripheral Whole Blood or Dried Blood Spot	21–28 Calendar Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MYO5A gene sequence", "Single-nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation [] Indications ["Suspected Griscelli syndrome type 1", "Family history of Griscelli syndrome type 1", "Evaluation of partial albinism and immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 62014-7 ICD-10: Q82.8 Clinical summary This test evaluates the MYO5A gene for mutations associated with Griscelli syndrome type 1.
TEST-5449 SPTBN5 Gene Neuronal Migration Disorder Genetic Test This genetic test evaluates the SPTBN5 gene for sequence variants and small deletions/duplications linked to neuronal migration disorders.	Peripheral whole blood (3–5 mL in EDTA)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SPTBN5 gene sequence variants", "Small deletions/duplications in SPTBN5 gene"] Parameters [] Preparation [] Indications ["Suspected SPTBN5-associated neuronal migration disorder", "Complex neurological presentations"] Measurement technique Confirm with laboratory Codes LOINC: 21523-3 ICD-10: Q04.8 Clinical summary This genetic test evaluates the SPTBN5 gene for sequence variants and small deletions/duplications linked to neuronal migration disorders.

Category overview

Next-Generation Sequencing: overview

Navigating complex, undiagnosed health challenges requires the most advanced genetic insights available to illuminate the best path forward. Within our elite Genetics department, Next-Generation Sequencing (NGS) provides an incredibly detailed, comprehensive reading of your DNA. By leveraging this state-of-the-art diagnostic technology, our high-throughput molecular screening helps uncover rare genetic variants and structural changes, 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 next-generation sequencing testing in UAE, arrange a secure home sample collection, or consult our dedicated medical genetics experts today.

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Use the test details as a conversation starter

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.