WGS Genetic Package

Whole Genome Sequencing (WGS) analysis is an advanced genetic technology that sequences an individual’s entire genome, meaning all genetic information in their DNA. This analysis provides a comprehensive insight into genes, helping to diagnose genetic diseases, detect rare mutations, and provide accurate medical recommendations. WGS is a powerful tool for fully understanding an individual’s or family members’ genetic health.

Analysis Details by Type:

Whole Genome Sequencing (Solo)

  • Sample: Blood
  • Results Duration: 30-45 days
  • Description:
    • Complete genome analysis for one person.
    • Detects genetic mutations that may affect health, chronic diseases, and the body’s response to medications.
    • Suitable for individuals with a family history of genetic diseases or unexplained symptoms.
    • Includes a detailed report with personalized medical recommendations.

Whole Genome Sequencing (Duo)

  • Sample: Blood (sample from two family members)
  • Results Duration: 30-45 days
  • Description:
    • Genome analysis for two individuals from the same family.
    • Helps compare genes between individuals to detect shared and individual mutations.
    • Useful for assessing genetic risks and providing early, accurate diagnosis.
    • Includes a detailed report for each individual with precise recommendations based on the results.

Whole Genome Sequencing (Trio)

  • Sample: Blood (3 family members, usually father, mother, and child)
  • Results Duration: 30-45 days
  • Description:
    • Complete genome analysis for three family members.
    • The best way to identify inherited and de novo mutations.
    • Contributes to accurate diagnosis of genetic diseases and provides personalized treatment recommendations.
    • Includes a comprehensive report detailing affected genes, health risks, and treatment options.

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