Genomapp: Raw DNA Analysis

Yenilikler

+ Minor bug fixes
+ General improvements

Bu uygulama hakkında

Make sense of your DNA test data and discover what your genes can tell you. Genomapp is a specialized genetic reference tool that cross-references your information with public databases of scientific studies to present findings in a visual, intuitive way.

Have you taken a DNA test? Did you know your genome has a lot to say? Want to learn more about your DNA? It is easier than you think.

*** Compatible with Ancestry.com & 23andMe

If you already have a raw DNA data file from services like 23andMe, AncestryDNA, FTDNA or MyHeritage, you can safely use it. Genomapp provides a personalized genetic exploration of your Ancestry.com or 23andMe results. Our tool quickly identifies thousands of genetic markers (SNPs) and shows health associations found in scientific evidence.

*** Privacy & Security (100% On-Device)

Protecting your privacy is our primary concern.
• Your data remains on your device.
• Genetic files are not stored on or uploaded to our servers.
• We do NOT share genetic data with third parties.

*** Ready to start?

Genomapp has a Demo mode. If you want to try the app or learn how it works, you can access a fully functional version for free.

*** What does Genomapp offer?

We offer 3 free reports and 3 premium reports:
• Complex Diseases: Literature on markers associated with multifactorial conditions (genetic and environmental factors).
• Inherited Conditions: Scientific records on markers related to diseases that are caused by mutations in a single gene.
• Pharmacological Compounds: Drug-marker associations found in peer-reviewed scientific studies.
• Genetic Traits: Characteristics or attributes expressed by your genes.
• Observable Signs: Understand markers related to physical signs.
• Blood Groups: Literature-relevant markers for transfusions or pregnancy.

*** Specialized genetic insights

• Methylation & MTHFR: Focused on metabolic health research, folate, and the MTHFR gene.
• Aging & Longevity: Explore the genetic markers mentioned in studies about aging mechanisms.

*** Certification

The app has been reviewed by the mHealth.cat Office (TIC Salut Social Foundation). This means that the quality of the content and the usefulness of the functions have been evaluated, meeting reliability requirements for health-related educational content.

*** Not diagnostic

Please note that Genomapp is a medical reference and educational tool. It is NOT for diagnostic use and does not provide medical advice or clinical decision support. Always consult your healthcare professional for any medical concerns.

*** Our database

Search our database of more than 9,500 conditions, 12,400 genes, and 180,000 genetic markers. Our tool facilitates access to research on a comprehensive list of conditions from scientific sources, including breast cancer, Alzheimer's, and Parkinson's. It also indexes literature for tumor suppressor genes such as BRCA, PTEN, and P53.

*** Easy to Understand

Genomapp displays your DNA markers in a friendly way. Export your personalized genetic reports to PDF for your personal research and records to take them anywhere.

*** Supported DNA Providers

We are constantly adding support for new providers. Currently, you can use files from 23andMe, Ancestry.com, Family Tree DNA (FTDNA), MyHeritage, Genes for Good, LivingDNA, Genographics (Geno 2.0), Tellmegen and other DTC genetic testing companies. Genomapp also supports VCF format files and specific schemes. (Note: VCF files from WES/WGS are currently not compatible).

Try Genomapp now and unlock your DNA analysis!

Genomapp: Raw DNA Analysis APK Nasıl İndirilir

1. Paket adını com.rfdevelopments.genomapp APK Downloader ana sayfasında girin.
2. Cihazınızın mimarisini seçin (modern cihazlar için ARM64 önerilir).
3. Birleştirilmiş APK dosyasını almak için İndir'e tıklayın.
4. APK'yı Android cihazınıza aktarın ve yükleyin.
5. Güncel Kalın: En sevdiğiniz uygulamaların en son güvenli sürümlerini aramak ve indirmek için düzenli olarak APK Downloader'ı ziyaret edin.