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Whole Exome Sequencing (WES)

Unlock the potential of your genetic information with our in-depth sequencing services
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Whole Exome Sequencing (WES)

Whole Exome Sequencing (WES)

Whole Exome Sequencing (WES) is a cutting-edge genetic testing service that sequences all the protein-coding regions of the genome, known as exons. By focusing on the exome, which contains the majority of known disease-causing mutations, WES provides a comprehensive and efficient method for diagnosing genetic conditions, identifying inherited disorders, and guiding personalized medical care.

Features:

  • Comprehensive Genetic Analysis: Sequences over 20,000 genes in the human genome, covering the exons where most genetic mutations that lead to diseases are found.
  • Accurate Diagnosis: Identifies genetic mutations that may be responsible for unexplained medical conditions, offering a precise diagnosis.
  • Personalized Treatment Guidance: Provides insights into the genetic basis of a condition, allowing for tailored treatment and management strategies.
  • Family Health Insights: Helps detect hereditary conditions that may affect family members, supporting informed family planning and proactive health management.
Whole Exome Sequencing (WES)

How It Works:

  1. Consultation: Begin with a consultation to discuss your medical history and determine if Whole Exome Sequencing is the right approach for your diagnostic needs.
  2. Sample Collection: A blood sample or saliva sample is collected for genetic analysis.
  3. Sequencing and Analysis: The sample is sent to a specialized laboratory, where advanced sequencing technology is used to analyze the exome and identify genetic variations.
  4. Results: Results are typically available within 4-6 weeks. Your healthcare provider will review and interpret the findings with you, explaining their significance and outlining potential next steps for treatment or further testing.

Who Should Consider Whole Exome Sequencing:

  • Unexplained Medical Conditions: Individuals with undiagnosed or complex medical conditions where a genetic cause is suspected.
  • Rare Disease Diagnosis: Patients with symptoms of a rare genetic disorder that has not been identified through other tests.
  • Family History of Genetic Disorders: Those with a family history of inherited diseases who want to understand their genetic risks.
  • Prenatal and Pediatric Concerns: Parents seeking to identify potential genetic conditions in their unborn or young children.

Frequently Asked Questions (FAQs)

What is Whole Exome Sequencing?
Whole Exome Sequencing is a genetic test that sequences all the protein-coding regions of the genome to identify mutations responsible for genetic conditions.
What happens if a mutation is found?
If a genetic mutation is identified, your healthcare provider will discuss its implications for your health and the next steps for treatment, management, or further testing.
Are there any risks associated with the testing?
WES is non-invasive, with minimal physical risks. However, the emotional impact of discovering a genetic mutation will be addressed with support and counseling as needed.