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This report does not include the Genome Sequencing test (to be purchased separately)

Paket mit allen Panels

Paket mit allen Panels

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

Dieses Produkt ist nur für Kunden gedacht, die bereits einen Dante-Genomtest erworben haben

Liste der enthaltenen Berichte:

Achromatopsie-Panel
ACMG-Panel
Acrodermatitis Enteropathica-Panel
Afibrinogenämie-Panel
Aicardi-Goutières-Syndrom-Gremium
Alagille-Syndrom-Gremium
Alkalische Phosphatase-Panel
Alport-Syndrom-Gremium
Amyloidogenes Transthyretin-Amyloidose-Panel
Panel zum Aneurysma-Risiko
Aortenaneurysma-Panel
Asthmaanfälligkeitsgremium
Gremium für Autismus und neurologische Entwicklungsstörungen
Autismus-Gremium
Autoimmunitätsgremium
Autoinflammatorisches Panel
Autophagie-Panel
Bardet-Biedl-Syndrom-Gremium
Brustkrebsgremium
Brugada-Syndrom-Gremium
CADASIL-Panel
Gremium für kardiometabolische Störungen
Gremium für Kardiomyopathien
Herz-Kreislauf-Panel
Carrier-Screening-Panel
Panel zur katecholaminergen polymorphen ventrikulären Tachykardie (CPVT).
Panel zu zerebralen kavernösen Fehlbildungen
Gremium für Charcot-Marie-Tooth-Krankheit
Chédiak-Higashi-Syndrom-Gremium
Gremium für chronische granulomatöse Erkrankungen
Gremium für chronische traumatische Enzephalopathie
Gremium für Ziliopathien
Zirkadianes Panel
COL7A1-Panel
Kombiniertes Hypophysenhormonmangel-Panel
Panel zur angeborenen Nebennierenhyperplasie
Panel zu angeborenen Katarakten
Panel „Angeborene Störungen der Glykosylierung“.
Panel zum angeborenen myasthenischen Syndrom
Panel für angeborene Neutropenie
Panel zum angeborenen Sucrase-Isomaltase-Mangel
Bindegewebspanel
Panel zu Störungen des Kupferstoffwechsels
Cowden-Syndrom-Gremium
Morbus Crohn-Gremium
Cutis Laxa-Panel
Panel für Mukoviszidose
Cystinurie-Panel
Zahnarztgremium
Dermatologisches Gremium
Diabetes-Gremium
Diamond-Blackfan-Anämie-Panel
Dilatative Kardiomyopathie-Panel
Panel für distale Myopathien
Panel „Dyskeratosis Congenita“.
Panel zu ektodermalen Dysplasien
Ectopia Lentis Panel
Ehlers-Danlos-Syndrom-Gremium
Endokrinologie-Gremium
Epidermolysis bullosa-Panel
Epilepsie-Gremium
Fallots Tetralogie-Panel
Panel zur familiären Hypercholesterinämie
Panel zur familiären intrahepatischen Cholestase
Fanconi-Anämie-Gremium
Panel zur weiblichen Unfruchtbarkeit
Panel für frontotemporale Demenz
Gastroenterologie-Gremium
Gilbert-Syndrom-Gremium
Glaukom-Panel
Glukokortikoid-Mangel-Panel
Glykogenspeicherkrankheiten
Gremium für Morbus Basedow
Gremium für Hörverlust und Taubheit
Hämatologie-Gremium
Panel zur hemiplegischen Migräne
Hämochromatose-Panel
Panel zur erblichen Amyloidose
Gremium für erblichen Krebs
Gremium für erblich bedingte Darmkrebserkrankungen
Panel zur hereditären hämorrhagischen Teleangiektasie
Gremium für erbliche Myopathien
Gremium für hereditäre Optikusneuropathie
Panel zur erblichen Pankreatitis
Panel zur hereditären spastischen Paraplegie (HSP).
Panel zur hereditären Vitreoretinopathie
Panel zum Hermansky-Pudlak-Syndrom
Panel zu Hyper-IgE-Syndromen
Gremium für hypertrophe Kardiomyopathie
Hypothyreose-Panel
Idiopathisches Kleinwuchsgremium
Gremium für entzündliche Darmerkrankungen
Panel zu Joubert- und Meckel-Gruber-Syndromen
Leigh-Syndrom-Gremium
Leukodystrophie-Panel
Long-QT-Syndrom-Panel
Panel zu lysosomalen Speicherstörungen
Panel zur männlichen Unfruchtbarkeit
Marfan-Syndrom-Gremium
Stoffwechselpanel
Panel „Methylierungsmechanismen“.
MODY-Panel
Multiple-Sklerose-Gremium
Nephrologie-Gremium
Neurofibromatose-Gremium
Neurologie-Gremium
Neuronales Ceroid-Lipofuszinose-Panel
Panel zur nicht-syndromalen Retinitis pigmentosa
Noonan-Syndrom-Gremium
Panel nuklearer mitochondrialer Gene
Gremium für Fettleibigkeit
Panel zur obstruktiven hypertrophen Kardiomyopathie
Onkologie-Gremium
Ophthalmologisches Gremium
Panel zu Arthrose und seltenen Knorpelerkrankungen
Osteogenesis Imperfecta-Panel
Osteopetrose-Panel
Gremium für oxidativen Stress
Palb2-Panel
Panel Parkinson – Alzheimer – Demenz
Parkinson-Gremium
Pädiatrie-Gremium
Pendred-Syndrom-Gremium
Panel für periodische Lähmungen
Gremium für polyzystische Nierenerkrankungen
Panel zum polyzystischen Ovarialsyndrom
Porphyrie-Panel
Panel „Vorzeitige ventrikuläre Kontraktionen“.
Panel zur primären Ziliardyskinesie
PRKDC-Panel
Pulmonale Hypertonie
Panel zu Lungensurfactant-Störungen
Pulmunologie-Gremium
RASopathies-Gremium
Panel zu wiederkehrenden Schwangerschaftsverlusten
Panel zu Störungen der Membran roter Blutkörperchen
Panel für rheumatoide Arthritis
Schizophrenie-Gremium
Seckel-Syndrom-Gremium
Panel für sekundären Hypogonadismus
Sensorisches Panel
Panel zum Serotonin-Stoffwechselmangel
Kurzes QT-Syndrom-Panel
Sjögren-Syndrom-Gremium
Gremium für Skelett- und Bindegewebserkrankungen
Panel zu Skelettdysplasien
Systemischer Lupus erythematodes Panel
Systemische Mastozytose-Panel
Tyrosinämie-Panel
Panel für Colitis ulcerosa
Panel zur Störung des Harnstoffzyklus
Valosinhaltiges Protein-Panel
Gremium für vaskuläre Demenz
Sehr langkettiges Acyl-CoA-Dehydrogenase-Mangel-Panel
Von Willebrand-Panel
WEST-Syndrom-Gremium
Wilson-Krankheitsgremium

Vollständige Details anzeigen
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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

  • 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
  • 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

  • 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