Whole Exome Sequencing Test (WES) - TRIOS - Price, Procedure

Introduction to Whole Exome Sequencing (WES)- TRIOS

Whole Exome Sequencing (WES) combined with TRIOS refers to a protein genetic testing approach used to identify the cause of a disease in a person and their family. WES focuses on sequencing the exome, the part of the genome containing instructions for building proteins. By analyzing these protein-coding regions, WES can help to identify mutations that might be causing a genetic disorder. 

The "Trio" aspect refers to analyzing the genetic data of the patient and both parents. It helps to identify mutations. If a mutation causing the disease is present in the child but not in either parent, it becomes a strong suspect. Your doctor may recommend the WES-TRIOS to identify the genetic basis of rare diseases with unknown causes. 

Test Details in Brief

Purpose of the Whole Exome Sequencing (WES)- TRIOS

The main purpose of Whole Exome Sequencing (WES) TRIOS is-

• To identify the genetic cause of a disease in a child by analyzing the DNA of the child and both biological parents.
• WES focuses on the exome, the region containing instructions for protein building. By sequencing this region in both the child and parents, WES-Trios can pinpoint mutations responsible for the child's condition, especially in rare diseases with unknown causes.
• Knowing the specific genetic mutation allows doctors to explore targeted therapies or tailor treatment approaches for the child. 

Preparation for the Whole Exome Sequencing (WES)- TRIOS

TRIOS itself is a DNA analysis and doesn't require specific preparation. However, here is what you need to know before the test- 

• You don't need to fast before the test. You can eat as usual before the test.
• Discuss your medications and supplements with your doctor before the test.

In addition, if you have doubts about the Whole Exome Sequencing (WES)- TRIOS, consult your healthcare provider beforehand.

The procedure of the Whole Exome Sequencing (WES)- TRIOS

• The phlebotomist will tie a band or tourniquet on the arm to make veins more visible and then clean the arm area with an antiseptic solution.
• Next, he will use a sterile needle to collect the blood sample in a vial or tube. You might feel a little pinch or discomfort during the sample collection.
• In the final step, the blood sample will be sent to the laboratory for analysis. 

What do the Whole Exome Sequencing (WES)- TRIOS reports indicate?

The Whole Exome Sequencing (WES) - TRIOS reports offer information about genetic disease causes. Here is what the test reports indicate- 

• De Novo Mutations- These new mutations arose in the child and weren't inherited from either parent. They can be strong indicators of the disease's cause.
• Inherited Mutations- In some cases, WES-Trios might reveal disease-causing mutations inherited from one or both parents, helping determine the inheritance pattern.

Consult your reports with healthcare experts; they can identify mutations and interpret your test results. 

Who should take the Whole Exome Sequencing (WES)- TRIOS?

Doctors recommend the Whole Exome Sequencing (WES) - TRIOS in specific situations. Here's what you must know:

• The child's particular symptoms and medical history
• Family history of genetic disorders
• People with Multiple Symptoms Suggesting a Genetic Cause

Whole Exome Sequencing (WES)- TRIOS price at Redcliffe Labs

The Exome Sequencing (WES) cost at Redcliffe Labs is INR 53000. You can consult your doctor and schedule your test online. The professional ensures you receive on-time test results and 100% correct reports. In addition, there are more than 3600+ diagnostic tests available, which you can choose at highly affordable prices. Don't wait for the symptoms to make the conditions more severe and worse. Book your ole Exome Sequencing (WES)- TRIOS today!

Whole Exome Sequencing Test (WES) - TRIOS Cost in Different Cities - Redcliffe Labs

WES-TRIOS: Unveiling Potential Genetic Causes

Whole Exome Sequencing (WES) - TRIOS is a powerful genetic testing approach highlighting the cause of suspected genetic disease. WES focuses on sequencing the exome, the part of the genome containing instructions for building proteins.