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Clinical Exome Trio Sequencing Test

12,000 د.إ

-20%

The Clinical Exome Trio Sequencing Test is a comprehensive genetic screening process designed to identify the genetic causes of inherited diseases within a family. Conducted at DNA Labs UAE, this advanced diagnostic test involves sequencing the exomes—the parts of the genome that encode proteins—of three individuals, typically the child and both parents. This trio approach significantly enhances the ability to pinpoint disease-causing mutations by comparing the child’s genetic information with that of the parents, thereby offering insights into the inheritance patterns and potential genetic disorders.

The test is particularly useful in cases where a child presents with symptoms of a genetic disorder that has not been diagnosed through other means. It can identify mutations in over 20,000 genes, covering a vast array of inherited conditions, including rare diseases that may not be detected through standard genetic tests. The Clinical Exome Trio Sequencing Test is invaluable for families seeking answers to complex genetic health puzzles, offering a pathway to targeted treatment options and personalized medical care.

The cost of the Clinical Exome Trio Sequencing Test at DNA Labs UAE is 12,000 AED. This investment covers the comprehensive analysis and detailed reporting necessary to understand the genetic underpinnings of inherited conditions, making it a critical step for families in pursuit of diagnosis, informed decision-making, and management of genetic disorders.

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  • This test is not intended for medical diagnosis or treatment
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Clinical Exome Trio Sequencing Test

Test Name: Clinical Exome Trio Sequencing Test

Components: Genetic testing method involving sequencing the exome of three individuals from the same family: the affected individual (proband) and their biological parents.

Price: AED 12,000.0

Sample Condition: Blood

Report Delivery Method: To be determined

Test Type: Doctor referral

Test Department: Genetic Lab

Pre Test Information

Clinical exome trio sequencing is a genetic testing method that involves sequencing the exome of three individuals from the same family: the affected individual (proband) and their biological parents. The exome is the portion of the genome that codes for proteins and is responsible for most genetic diseases.

Test Details

By sequencing the exomes of all three individuals, genetic variations can be identified and compared to determine if the proband inherited a disease-causing variant from one or both parents. This information can help diagnose genetic disorders and inform treatment options.

Clinical exome trio sequencing is particularly useful for diagnosing rare genetic diseases that may not be identified through other testing methods. It can also help identify genetic risks for future pregnancies and inform genetic counseling.

Test Name Clinical Exome Trio Sequencing Test
Components
Price 12000.0 AED
Sample Condition Blood
Report Delivery
Method
Test type
Doctor
Test Department:
Pre Test Information
Test Details

Clinical exome trio sequencing is a genetic testing method that involves sequencing the exome of three individuals from the same family: the affected individual (proband) and their biological parents. The exome is the portion of the genome that codes for proteins and is responsible for most genetic diseases.

By sequencing the exomes of all three individuals, genetic variations can be identified and compared to determine if the proband inherited a disease-causing variant from one or both parents. This information can help diagnose genetic disorders and inform treatment options.

Clinical exome trio sequencing is particularly useful for diagnosing rare genetic diseases that may not be identified through other testing methods. It can also help identify genetic risks for future pregnancies and inform genetic counseling.