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Whole Genome Sequencing

Ensuring a healthy and successful pregnancy

What is Diagnostic Testing by WGS

Whole Genome Sequencing (WGS) involves decoding the entire DNA sequence of an individual’s genome. This comprehensive approach examines both coding and non-coding regions, providing a detailed blueprint of the genetic material. This comprehensive genetic test allows for the detection of variants in coding and non-coding regions, in addition to structural variants, eliminating the need for multiple genetic tests. WGS offers an unparalleled depth of insight into your unique genetic makeup.

Indicators of Inherited Disease Testing by WGS

  • Exploring a suspected genetic condition despite an initial negative WES result
  • Suspected rare genetic diseases or disorders where the genetic basis is not well understood
  • Unraveling Complex Genetic Disorders
  • Couples with a family history of genetic disorders planning to have children
  • As part of proactive health management for individuals interested in understanding their genetic predispositions

Benefits of WGS

  • Comprehensive Genomic Analysis: Encompassing exons, noncoding regions, and structural variants for an all-encompassing diagnostic approach, negating the need for multiple tests
  • Fosters breakthroughs in gene research and discovery
  • Potential for additional insights into pharmacogenomics data reporting
  • Guiding personalized therapies and treatments

Why Viafet

  • Comprehensive Genomic Analysis: Encompassing exons, noncoding regions, and structural variants for an all-encompassing diagnostic approach, negating the need for multiple tests
  • Fosters breakthroughs in gene research and discovery
  • Potential for additional insights into pharmacogenomics data reporting
  • Guiding personalized therapies and treatments

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