Whole Genome Sequencing (WES) Test - Price, Purpose, & More

Introduction to the Whole Genome Sequencing Test

The whole genome sequencing test is a comprehensive method for analyzing entire genomes. The test has been instrumental in identifying genetic disorders and describing the mutations that drive cancer progression and associated diseases. Whole genome sequencing is a powerful way to determine the order of DNA building blocks in an individual's genetic code. So, your doctors may suggest a whole genome sequencing test when they suspect a family history of disease or are experiencing symptoms. For children whose diseases have not been diagnosed, the WGS test might reveal an underlying diagnosis, such as intellectual disability, severe learning problems, hearing and vision problems, heart and lung complications, and severe unexplained illness. Early diagnosis helps doctors with better management, allowing precision medicine to provide the utmost care for these vulnerable patients.

If your doctor has suggested the test, Redcliffe Labs is the best omnichannel pan-India diagnostic service provider for booking a WGS test at home. Our team of trained medical professionals, or phlebotomists, provides a doorstep blood sample collection service. So, book a whole genome sequencing test with Healthy India Ki Trusted Lab, Redcliffe Labs. 

Test Details:

When do I need a whole genome sequencing test? 

The test is often recommended by doctors when they suspect you are suffering from inherited disorders. When they discover symptoms suggestive of genetic mutations related to congenital disabilities or disease outbreaks, they may suggest the WGS test to confirm the same. Such symptoms include: 

• Development delays: When a patient complains about developmental delays in their child compared to other children the same age, it includes delays in rolling over, sitting up, crawling, issues with social skills, etc.; the healthcare provider may suggest the whole genome sequencing test. 
• Hearing and vision impairment: Developmental delays alone cannot confirm a need for the WGS test. However, for other symptoms, such as hearing and vision impairment, the WGS test helps individuals understand their genetic basis for hearing loss. Early detection allows for proactive measures, helps them understand their risk, and helps them make informed decisions about their hearing health. 

Besides developmental delays and hearing and vision impairment, there are several other conditions where your healthcare provider may suggest the test, such as: 

Other reasons when a doctor prompts the need for a whole genome sequencing test

• Monitor Intestinal Issues: The test can provide a more accurate diagnosis for individuals with a poorly functioning immune system. The whole genome sequencing test has been used to identify bacterial species and strains and is also helpful in determining resistance to antibiotics based on genetic information.
• Seizures: This is a complex genetic test that reveals the whole DNA code to look for changes in genes linked to epilepsy.
• Unexplained Illness: There are some unexplained illnesses for which the WGS might prove beneficial, such as intellectual disability, severe learning problems, or sudden childhood deaths. 

No matter the reason, if your doctor has prescribed a whole genome sequencing test based on symptoms, potential risk factors, or other conditions, getting tested in time is important for evaluating genetic disorders and associated diseases and taking appropriate measures accordingly. 

What preparations are required for the whole genome sequencing test?

The WGS DNA test usually requires no preparation. However, following a few guidelines can help you get accurate test results. 

• The WGS test requires no fasting. You can drink or eat normally before the test. 
• You must follow the instructions carefully provided by your healthcare provider to expect accurate test results. 
• If you are on some prescribed or non-prescribed medicines, it is advisable to inform your doctor so that the medicine ingredients do not influence the test results. 

If you have any questions about the test preparations, talk to your healthcare provider to ensure the measurements are appropriately taken and the test results are accurate. 

What is the procedure for the whole genome sequencing test? 

The WGS test is simple and involves the following steps: 

• It is advisable to wear something with short sleeves, as the phlebotomist will take the blood from the vein in your arm. He may also tie a band around your arm and ask you to make a fist, ensuring the vein is properly visible. 
• The phlebotomist will then clean the site with a disinfectant to prevent infection and insert a sterile syringe into your vein to draw the blood. 
• Once the blood is taken, he will remove the syringe and apply a bandage to the site to prevent bleeding or infection. 
• Lastly, he will transfer the blood sample to the vial and send it to the laboratory for analysis. 

The entire procedure is simple and hassle-free. However, inserting and removing a needle may cause a slight pain or bruise on the punctured area, but it will disappear after a few days. Kindly seek medical assistance if the symptoms remain visible. 

What does the whole genome sequencing test result mean?

A whole genome sequencing test uncovers approximately all genome DNA variation, including coding and non-coding regions. It is a very special type of molecular diagnostic that maps out the complete DNA code of the tumor, revealing all abnormalities at once. 

The results of genetic tests are only sometimes understandable, which means that you should ask your healthcare provider questions about the potential meaning of the results. While interpreting the WGS test report, doctors consider a person’s family medical history and the type of genetic test done. 

Book the Whole Genome Sequencing Test at an Affordable Whole Genome Sequencing Test Price!

When diagnosing any genetic disorder or tracking disease outbreaks, a delay should never be made from your end to avoid drastic outcomes. Hence, if your healthcare provider has recommended the whole genome sequencing test, you can book now with Redcliffe Labs. You can get tested at an affordable whole genome sequencing price of Rs. 130000. Enjoy convenient blood test home collection, express slots to get your sample picked up within 45 minutes, and accurate test reports within a given time frame. So, why wait? Book a whole genome sequencing test with us now. 

Whole Genome Sequencing (WGS) Test Cost in Different Cities - Redcliffe Labs

Note: We also offer Whole Genome Sequencing (WGS) Test PAN India. Please call the number 8988988787 to check the availability of our services in your area.