Couple Whole Exome Sequencing (WES) is an advanced genetic test that analyzes the protein-coding regions (exons) of both partners' DNA. It helps identify disease-causing genetic variants and determines whether the couple carries mutations that could increase the risk of passing inherited disorders to their children.
Why is this test recommended?
Detects carrier status for thousands of inherited genetic disorders.
Assesses reproductive risk before pregnancy or during family planning.
Supports informed decisions regarding conception and prenatal care.
Helps identify rare genetic conditions not covered by routine carrier screening.
Who should consider this test?
Couples planning a pregnancy.
Couples with a family history of inherited disorders.
Couples with recurrent miscarriages or infertility.
Consanguineous (blood-related) couples.
Couples with a previously affected child.
Sample Required
Peripheral Blood (EDTA) from both partners.
Benefits
Comprehensive analysis of over 20,000 genes.
Identifies rare and clinically significant variants.
Enables personalized genetic counseling.
Helps reduce the risk of inherited diseases in future generations.
Provides valuable information for reproductive planning.
Interpretation
Negative: No clinically significant pathogenic variants detected.
Carrier Positive: One or both partners carry variants associated with inherited disorders.
At-Risk Couple: Both partners carry pathogenic variants in the same recessive gene, increasing the chance of having an affected child.
Results should always be interpreted alongside genetic counseling.
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COUPLE Whole Exome Sequencing (WES)
Plan Parenthood with Confidence! ❤️🧬
✔ Detects inherited genetic disorders in both partners ✔ Comprehensive exome analysis ✔ Supports healthy family planning ✔ Recommended before pregnancy & IVF
Early genetic insights lead to informed decisions.