Overview
The 2x150 Hiseq Sequencing test is a high-throughput next-generation sequencing (NGS) technique that reads 150 base pairs from both ends of DNA fragments, generating 300 base pair reads. This method is widely used in clinical genetics to identify disease-causing mutations, diagnose genetic disorders, and guide personalized treatment. At DNA Labs India, we offer this comprehensive test at an affordable cost of INR 7500, covering 3GB of sequencing data. The test is performed on extracted DNA samples, and results are typically available within 4 weeks. Our expert geneticists and bioinformaticians analyze the data to provide actionable insights, including identification of pathogenic variants, carrier status, and pharmacogenomic implications. This test is ideal for individuals with unexplained symptoms, a family history of genetic disorders, or those seeking personalized health information. With free home sample collection available across major cities in India, DNA Labs India makes advanced genetic testing accessible and convenient.
To be completed — reclassified from Tests on 2026-11-13.
The purpose of the 2x150 Hiseq Sequencing test is to detect genetic variations that may be responsible for a patient's symptoms or disease. It helps in: 1) Diagnosing genetic disorders, 2) Identifying carrier status for recessive conditions, 3) Guiding treatment decisions (pharmacogenomics), 4) Assessing risk for hereditary cancers, 5) Providing information for family planning, 6) Understanding unexplained developmental delays or congenital anomalies.
Sample requirements
What to send us
Deliverables & turnaround
What you receive
Turnaround: Results are typically available within 4 weeks from the time the sample is received at the laboratory.
Pricing
Transparent pricing
| Option | Turnaround | Price (INR) | Unit |
|---|---|---|---|
| Standard | Results are typically available within 4... | ₹7,500 | per sample |
Limitations & precautions
What this service cannot do
Questions customers ask
Frequently asked questions
What is 2x150 Hiseq Sequencing?
2x150 Hiseq Sequencing is a next-generation sequencing method that reads 150 base pairs from both ends of DNA fragments, producing 300 base pair reads. It is used for high-throughput genetic analysis.
What is the cost of the test?
The test costs INR 7500, which includes sequencing of 3GB data and a comprehensive report.
What is the turnaround time?
Results are typically available within 4 weeks after sample submission.
What sample is required?
Extracted DNA is required. We provide a free home sample collection service for blood or saliva samples.
Is fasting required?
No, fasting is not required for this test.
What kind of results will I get?
You will receive a report detailing any disease-causing mutations, carrier status, and potential health risks, along with recommendations for personalized treatment.
Can this test detect all genetic disorders?
No, it may not detect all types of mutations, such as large deletions or repeat expansions. It is best used for identifying single nucleotide variants and small indels in coding regions.
Is home sample collection available?
Yes, we offer free home sample collection for online bookings across many cities in India.
How should I prepare for the test?
No special preparation is needed. Just ensure you provide a good quality sample as per instructions.
Will my insurance cover this test?
Insurance coverage varies. Please check with your insurance provider. We also offer affordable self-pay options.
What is the difference between this and Whole Exome Sequencing?
This test may be a targeted or limited sequencing approach, while Whole Exome Sequencing covers all coding regions of the genome. The choice depends on clinical indication.
How accurate is this test?
The test is highly accurate for detecting variants in the targeted regions, with a mean depth of coverage ?30x. However, all clinically significant variants are confirmed by Sanger sequencing.
Continue here
Related services
Enquiry
Request a quote or ask a question
Editorial accountability