• All Panels Package - Dante Labs World
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This report does not include the Genome Sequencing test (to be purchased separately)

All Panels Package

All Panels Package

Dhs. 863.00 AED
Dhs. 2,162.00 AED Dhs. 863.00 AED
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✔️ Add-on Report to your Genome Test

List of Reports included :


Achromatopsia Panel
ACMG Panel
Acrodermatitis Enteropathica Panel
Acute Hepatic Porphyria Report
Afibrinogenemia Panel
Aicardi-Goutières Syndrome Panel
Alagille Syndrome Panel
Alkaline Phosphatase Panel
Alport Syndrome Panel
Amyloidogenic transthyretin amyloidosis Panel
Aneurysm risk Panel
Aortic Aneurysm Panel
Asthma Susceptibility Panel
Autism and Neurodevelopmental Disorders Panel
Autism Panel
Autoimmunity Panel
Autoinflammatory Panel
Autophagy Panel
Bardet Biedl Syndrome Panel
Bartter and Gitelman's Syndromes Report
Breast Cancer Panel
Brugada Syndrome Panel
CADASIL Panel
Cardiometabolic Disorders Panel
Cardiomyopathies Panel
Cardiovascular Panel
Carrier Screening Panel
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel
Cerebral Amyloid Angiopathy Report
Cerebral cavernous malformations Panel
Charcot-Marie-Tooth Disease Panel
Chédiak-Higashi Syndrome Panel
Chronic Granulomatous Disease Panel
Chronic Traumatic Encephalopathy Panel
Ciliopathies Panel
Circadian Panel
COL7A1 Panel
Combined Pituitary Hormone Deficiency Panel
Congenital Adrenal Hyperplasia Panel
Congenital Cataracts Panel
Congenital Disorders of Glycosylation Panel
Congenital Myasthenic Syndrome Panel
Congenital Neutropenia Panel
Congenital Sucrase-Isomaltase Deficiency Panel
Connective Tissue Panel
Copper Metabolism Disorders Panel
Cowden Syndrome Panel
Crohn Disease Panel
Cutis Laxa Panel
Cystic Fibrosis Panel
Cystinuria Panel
Dentist Panel
Dermatology Panel
Diabetes Panel
Diamond-Blackfan Anemia Panel
Dilated Cardiomyopathy Panel
Distal Myopathies Panel
Dyskeratosis Congenita Panel
Dystonia, Myotonia and Paroxysmal Dyskinesia Report
Ectodermal Dysplasias Panel
Ectopia Lentis Panel
Ehlers-Danlos Syndrome Panel
Endocrinology Panel
Epidermolysis Bullosa Panel
Epilepsy Panel
Erythropoietin Receptor Report
Fallot's Tetralogy Panel
Familial Hypercholesterolemia Panel
Familial Intrahepatic Cholestasi Panel
Fanconi Anemia Panel
Female infertility Panel
Focal Segmental Glomerulosclerosis and Complement Genetic Study Report
Frontotemporal Dementia Panel
Gastroenterology Panel
Gilbert Syndrome Panel
Glaucoma Panel
Glucocorticoid Deficiency Panel
Glycogen Storage Diseases
Graves' Disease Panel
Hearing Loss and Deafness Panel
Hematology Panel
Hemiplegic Migraine Panel
Hemochromatosis Panel
Hemolytic Uremic Syndrome and Autosomal Dominant Interstitial Nephritis Reports
Hereditary Amyloidosis Panel
Hereditary Cancer Panel
Hereditary Colorectal Cancers Panel
Hereditary Hemorrhagic Telangiectasia Panel
Hereditary Kidney Cancers Report
Hereditary Myopathies Panel
Hereditary Optic Neuropathy Panel
Hereditary Pancreatitis Panel
Hereditary Prostate Cancer Report
Hereditary Spastic Paraplegia (HSP) Panel
Hereditary Vitreoretinopathy Panel
Hermansky-Pudlak syndrome Panel
Hyper IgE syndromes Panel
Hypertrophic Cardiomyopathy Panel
Hypothyroidism Panel
Idiopathic short stature Panel
Inflammatory Bowel Disease Panel
Joubert and Meckel-Gruber syndromes Panel
Leigh Syndrome Panel
Leukodystrophy Panel
Long QT Syndrome Panel
Lysosomal Storage Disorders Panel
Male infertility Panel
Marfan Syndrome Panel
McArdle Disease Report
Metabolic Panel
Methylation Mechanisms Panel
MODY Panel
Multiple Sclerosis Panel
Nephrology Panel
Neurofibromatosis Panel
Neurology Panel
Neuronal Ceroid Lipofuscinosis Panel
Non-syndromic Retinitis Pigmentosa Panel
Noonan Syndrome Panel
Nuclear Mitochondrial Genes Panel
Obesity Panel
Obstructive Hypertrophic Cardiomyopathy Panel
Oncology Panel
Ophthalmology Panel
Osteoarthritis and rare cartilage diseases Panel
Osteogenesis Imperfecta Panel
Osteopetrosis Panel
Oxidative Stress Panel
Palb2 Panel
Parkinson - Alzheimer - Dementia Panel
Parkinson's Disease Panel
Pediatric Panel
Pendred Syndrome Panel
Periodic Paralysis Panel
Polycystic Kidney Disease Panel
Polycystic Ovary Syndrome Panel
Porphyria Panel
Premature Ventricular Contractions Panel
Primary Ciliary Dyskinesia Panel
Primary Immunodeficiency Report
PRKDC Panel
Pulmonary Arterial Hypertension
Pulmonary Surfactant Dysfunctions Panel
Pulmunology Panel
RASopathies Panel
Recurrent pregnancy loss Panel
Red Blood Cell Membrane Disorders Panel
Rheumatoid Arthritis Panel
Schizophrenia Panel
Seckel Syndrome Panel
Secondary Hypogonadism Panel
Sensory Panel
Serotonin Metabolism Deficiency Panel
Short QT Syndrome Panel
Sjögren’s Syndrome Panel
Skeletal and Connective Tissue Disorders Panel
Skeletal Dysplasias Panel
Systemic lupus erythematosus Panel
Systemic mastocytosis Panel
Type 4 Spastic Paraplegia Report
Tyrosinemia Panel
Ulcerative Colitis Panel
Urea cycle disorder Panel
Valosin-Containing Protein Panel
Vascular Dementia Panel
Very long chain acyl-CoA dehydrogenase deficiency Panel
Von Willebrand Panel
Waardenburg Syndrome Panel
WEST Syndrome Panel
Wilson Disease Panel

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Your blueprint for a healthier life

  • Actionable Insights

    Receive a complete blueprint to anticipate health risks years before symptoms appear, get a personalized prevention plan and make informed choices for a longer, healthier life

  • Your full DNA

    Get the full picture, not a snapshot. The genome is your full DNA and has 10,000 times more data than most wellness and ancestry DNA tests that analyze less than 0.01% of your DNA.

  • A lifelong investment

    Your DNA never changes, but science advances exponentially. Receive updates whenever new discoveries emerge—no need for repeated tests. Today's investment is tomorrow's insight

Thousands of lives transformed by the Dante Genome

Join the thousands whose life was transformed by the Dante Genome.

Better medical support, better clinical insights, real action plans, a new tool for your doctor

Why Dante

  • Superior Health Insights

    You receive actionable insights and a plan to take real steps in your life. Our reports provide real guidance on how to improve your healt and well being

  • Deeper Science

    From rare diseases to neurology, from longevity to family planning. Our sceince and expertise help solve more problems. Our reports cover a wide range of health uses

  • 10,000 Times More Data

    Unlock the power of 100% of your DNA. The genome has 10,000 times more data than most wellness and ancestry DNA test that analyze less than 0.01% of your DNA

Superior Insights

  • Fully personalized reports
  • Actionable insights
  • Genetic counseling (extra)
  • Proactive screening report
  • Future updates
  • Simple sample collection kit
  • Free worldwide shipping
  • 30X Coverage
  • Full ownership of your data
  • GDPR privacy protection

Deeper Science

  • 1 Million Genomic Reports

    We generated more than 1.3 million genomic reports based on whole genome delivering superior results to users in 100 different countries

  • AI Powered Interpretation

    From the AI Genome Chat to our automated updates, the Dante Genome offers actionable health insights across your entire body

  • State-of-the-art Sequencing Lab

    We run a clinical multiomics sequencing lab with ISO9001 accreditation and multiple Next Generation Sequencing workflows

10,000 times more data

  • The Dante Genome Test

    Whole genome sequencing is the analysis of your full DNA - 100% of your DNA - the most complete and comprehensive and complex DNA test available.

    We provide whole genome sequencing and generate and analyze 10,000 times more data than traditional genetic tests that only analyze less than 0.01% of your DNA.

  • Traditional DNA Tests

    Traditionally, genetic tests are limited to examining specific genes or regions of the genome, missing more than 99.9% of your DNA.

    These inferior DNA tests are based on an old technology called microarray but provide only limited insights.

FAQ

What is included in the test?

You receive your full whole genome data (FASTQ, BAM and VCF files), and AI reports. You can get additional reports anytime, without the need to re-send your sample.

What is 30X coverage?

30X coverage is the gold standard in clinical grade whole genome sequencing, offering high-confidence variant calls and interpretation. A 30X whole genome is a superior test than a low pass genome or a microarray

Will I get my raw data?

Yes - FASTQ, BAM, and VCF files are included

Who owns my DNA data?

You own your data. 100% of it. 100% of the time.

How do I collect my sample?

You will receive a saliva sample collection kit at home. Painless. Non invasive. Easy to use. And also a prepaid return label to send the sample back to our lab

What about shipping?

Shipping is free. Everywhere in the world. You will receive a return label with your kit to send your sample back to our lab

Do you work with companies?

If you have an interesting project or would like to speak with our B2B Team, please contact us. We provide genomics and multi-omics services to universities, biotech companies, clinics and hospitals