Gene Sequencing

• The WES test is recommended for individuals with genetic disorders, undiagnosed symptoms, developmental delays, or planning to have children.

• The WES blood test is taken to identify genetic mutations that may cause or contribute to disease and to provide information for diagnosis, treatment, and family planning.

• WES test helps identify genetic mutations that may cause or contribute to disease. It also helps to detect rare genetic disorders and provides information for diagnosis, treatment, and family planning.

Whole Exome Sequencing Test

Whole Exome Sequencing (WES) is a genetic test that analyzes the protein-coding regions of a person’s DNA.

These regions, also known as exons, comprise only about 1-2% of the genome but contain most known disease-causing mutations. By analyzing these regions, the WES test can provide valuable information about a person’s risk of inherited diseases and help diagnose rare genetic disorders.

The test involves collecting a small sample of DNA, which is then sequenced using advanced technology to identify any variations or mutations.

WES Test is Recommended For:

• Individuals with a personal or family history of genetic disorders.
• Patients with symptoms of an undiagnosed genetic condition.
• Infants or children with developmental delays or intellectual disabilities.
• Couples planning to have children who are carriers of genetic mutations.