x

Whole Genome Sequencing (WGS)

Providing answers to complex genetic challenges through comprehensive DNA sequencing in 4-6 weeks

NoorDx’s next generation Whole Genome Sequencing

Whole Genome Sequencing (WGS) is the most comprehensive genetic lab test. It examines up to 98% of a patient’s DNA making it a powerful tool that can detect almost all disease-causing genetic variations.

 

Whether a patient is new, or has been suffering undiagnosed or misdiagnosed for years, Whole Genome Sequencing testing is the one-stop clinical genetic test that can help find the cause of the genetic disorder.

new-thumb1
Whole-Genome-Sequencing-(WGS)
Previous
Next

We recommend a Whole Genome Sequencing lab test when:

 

  • Symptoms are complex or unspecific and a broad range phenotypic features is exhibited
  • Other testing options have not led to conclusive diagnosis
  • Rapid diagnosis is necessary
  • Standard (4-6 weeks)
  • Urgent (10 working days)

At NoorDx we are there for you every step of the way. We are always on hand to guide you throughout your genetics journey, from helping you choose the most appropriate test, to understanding the results, and directing you to the most effective precision treatment options. As the leading and most trusted genetics testing lab in the MENA region, we partner with you to find breakthrough solutions quickly and effectively.

 

Our expert team of technicians and scientists understand both Arabic and English, removing any barriers that may block the path to better health and improved quality of life.

 

At NoorDx, we are working to advance disease and gene research and help you find solutions. We are committed to innovating and using our data for scientific discovery that will enable a better quality of life for all in the Kingdom and the MENA region.

Limitations
  • A negative result does not exclude a genetic cause of the disease.
  • In some cases, variants may not be identified due to technical limitations caused by the presence of pseudogenes, repetitive, or homologous regions.
  • This test is not intended to detect low-level mosaic or somatic variants, gene conversion events, complex inversions, translocations, DNA (mtDNA) mutations, or repeat expansions.
  • Interpretation of this test result may be impacted if this patient has had an allogeneic stem cell transplantation.

Why choose NoorDx?

Rapid

Delivering results in days

Innovative

Pioneering solutions in genomics testing to save lives

Confidential

Providing the highest levels of patient privacy and advanced data security

World-class

Granting access to a team of expert genetics within our state-of-the-art lab