Whole Genome Sequencing MAX

  • Whole Genome Sequencing (MAX) is an exceptionally thorough genetic laboratory test that evaluates up to 98% of a patient’s DNA. This highly robust tool has the ability to detect nearly all genetic variations that contribute to disease.
  • Whether a patient is newly experiencing symptoms or has endured years of undiagnosedor misdiagnosed conditions, Whole Genome Sequencing testing serves as a comprehensive clinical genetic test that can pinpoint the underlying cause of genetic disorders.
  • Symptoms are complex or unspecific and a broad range of phenotypic features is exhibited.
  • Other testing options have not led to conclusive diagnosis.
  • Rapid diagnosis is necessary.