Discover ~85% of all known genetic diseases and ~15% genetic variations that affect gene activity.

Discover ~85% of all known genetic diseases.

3 months

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Whole Genome Sequencing

  • Most comprehensive human genome sequencing technology
  • Allow detection of protein-coding genes (85%) and non-protein coding genes (15%) which related to genetic diseases
  • Analyze ALL of your genetic raw data (allow detection of rare diseases)

2 months

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WES Advanced

Whole Exome Sequencing Advanced

  • Combines both WES & microarray-based genotyping tests
  • Enables detection of genetic variants in both protein-coding genes (WES) and intronic regions (Microarray)
  • Analyze ALL of your genetic raw data (allow detection of rare diseases)

TAT: Turnaround Time


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Personalized Report

Receive a personalized report tailored to you based on your unique genome

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Nutrition & Diet Plan

Discover what vitamins and nutrients that suit you the best and plan for healthy eating

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Professional Consultation

Get consulted by our healthcare providers

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Exercise & Fitness

Discover how you response to certain exercise training and risk of injury

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NexTx Platform

Manage your health and get yourself educated

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Discover your genetic predisposition to diseases including rare diseases

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Discover how you respond to certain drugs

Here are some of Rare Disorders / Diseases that can be discovered by our Nextx DNA test service:
1. Achondroplasia (Dwarfism) 2. Cancers a. Breast cancer b. Colorectal cancer c. Ovarian cancer 3. Congenital Disorder of Glycosilation (CDG) Type 1b 4. Duchenne muscular dystrophy (DMD) 5. Fragile-X syndrome 6. Hypoplastic left heart syndrome (HLHS) 7. Inborn errors of metabolism Syndromes 8. Leber congenital amaurosis 9. Long segment tracheal stenosis 10. Lynch syndrome 11. Lysosomal Storage Disorders a. Sly Syndrome (MPS VII) (LSD) b. Pompe's disease (LSD) c. Hunter Syndrome (MPS II) (LSD) d. Maroteaux-Lamy syndrome (MPSVI) disease (LSD) e. Morquio Syndrome (MPS IV) disease (LSD) f. Mucopolysaccharidosis Chromosomal abnormalities (Hurler Syndrome) 12. Maple Syrup Urine Disease 13. Marfan syndrome 14. Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes 15. Neuroblastoma 16. Osteogenesis imperfecta 17. Prader-Willi syndrome 18. Primary ciliary dyskinesia (PCD) 19. Severe combined immunodeficiency disease (SCID) 20. Type 1 diabetes