• Nuclear Mitochondrial Genes Report - Dante Labs World
1 1

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

Panel nuklearer mitochondrialer Gene

Panel nuklearer mitochondrialer Gene

€29.00 EUR
€29.00 EUR
Sale Ausverkauft

✔️ Add-on Report to your Genome Test

Dieses Produkt ist nur für Kunden gedacht, die bereits eines gekauft haben Dante-Genomtest

Die in diesem Panel analysierten genetischen Varianten stehen in engem Zusammenhang mit schwerwiegenden mitochondrialen Erkrankungen oder sind möglicherweise deren Ursache
Das Nuclear Mitochondrial Genes Panel wird verwendet, um nukleare genetische Varianten zu identifizieren, die mit mitochondrialen Erkrankungen verbunden sind, einer Gruppe seltener genetischer Störungen, die die energieproduzierenden Organellen in Zellen beeinträchtigen. Mitochondriale Erkrankungen können jedes Organ oder Gewebe im Körper betreffen und eine Vielzahl von Symptomen verursachen, darunter Muskelschwäche, Entwicklungsverzögerung und Kardiomyopathien. Mitochondriale Erkrankungen, die durch nukleare Genmutationen verursacht werden, können die Funktion, den Stoffwechsel und die Stabilität der Mitochondrien beeinträchtigen.
Dieses Panel richtet sich an Personen mit einer familiären Vorgeschichte von mitochondrialen Erkrankungen, die durch Kernmutationen verursacht werden, oder an Personen mit Symptomen dieser Erkrankung, wie Muskelschwäche, Entwicklungsverzögerung und Kardiomyopathien. Gentests können eine Diagnose bestätigen, Informationen über die Schwere und das Fortschreiten der Erkrankung liefern und als Grundlage für Behandlungs- und Managemententscheidungen dienen. Tests können auch Entscheidungen zur Familienplanung treffen und nicht betroffenen Familienmitgliedern Sicherheit geben.

Die Analyse berücksichtigt die Mutation der Keimbahn-DNA und untersucht SNP- und Indel-Mutationen bis zu 150 bp.

  • Verfügbar in weniger als 24 Stunden
  • Basierend auf der Sequenzierung des gesamten Genoms
  • Mehr als 90 Gene analysiert
  • Untersucht SNP- und Indel-Mutationen bis zu 150 bp

Liste der Hauptbedingungen:
  • Autosomal-dominante Optikusatrophie
  • Alpers-Huttenlocher-Syndrom
  • Leigh-Syndrom
Vollständige Details anzeigen
  • Financial Times logo on a white background

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