Clinical Exome Sequencing for Couple Test
Test Name: Clinical Exome Sequencing for Couple Test
Components: Protein-coding regions of the genome (exons)
Price: 7500.0 AED
Sample Condition: Blood
Report Delivery Method: To be discussed with the doctor
Test Type: Genetic test
Test Department: DNA Labs UAE
Pre Test Information
Clinical exome sequencing is a genetic test that analyzes the protein-coding regions of the genome, which are called exons. These regions contain the majority of disease-causing mutations. Clinical exome sequencing can be used to diagnose genetic disorders in couples who are planning to have children or who have a family history of genetic disease.
Test Details
The process of clinical exome sequencing involves obtaining a blood or saliva sample from each member of the couple. The DNA is then extracted from the sample and sequenced using next-generation sequencing technology. The resulting data is analyzed to identify any genetic variants that may be associated with disease.
The results of clinical exome sequencing can provide valuable information for couples who are planning to have children. If a genetic variant is identified that is associated with a disease, the couple can make informed decisions about their reproductive options. For example, they may choose to undergo in vitro fertilization with pre-implantation genetic testing to select embryos that do not carry the disease-causing variant.
Overall, clinical exome sequencing can be a useful tool for couples who are concerned about the risk of genetic disease in their future children. However, it is important to note that not all genetic variants are associated with disease, and the interpretation of genetic test results can be complex. It is recommended that couples discuss the potential benefits and limitations of clinical exome sequencing with a genetic counselor before undergoing testing.
Test Name | Clinical Exome Sequencing for Couple Test |
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Components | |
Price | 7500.0 AED |
Sample Condition | Blood |
Report Delivery | |
Method | |
Test type | |
Doctor | |
Test Department: | |
Pre Test Information | |
Test Details | Clinical exome sequencing is a genetic test that analyzes the protein-coding regions of the genome, which are called exons. These regions contain the majority of disease-causing mutations. Clinical exome sequencing can be used to diagnose genetic disorders in couples who are planning to have children or who have a family history of genetic disease. The process of clinical exome sequencing involves obtaining a blood or saliva sample from each member of the couple. The DNA is then extracted from the sample and sequenced using next-generation sequencing technology. The resulting data is analyzed to identify any genetic variants that may be associated with disease. The results of clinical exome sequencing can provide valuable information for couples who are planning to have children. If a genetic variant is identified that is associated with a disease, the couple can make informed decisions about their reproductive options. For example, they may choose to undergo in vitro fertilization with pre-implantation genetic testing to select embryos that do not carry the disease-causing variant. Overall, clinical exome sequencing can be a useful tool for couples who are concerned about the risk of genetic disease in their future children. However, it is important to note that not all genetic variants are associated with disease, and the interpretation of genetic test results can be complex. It is recommended that couples discuss the potential benefits and limitations of clinical exome sequencing with a genetic counselor before undergoing testing. |