2x150 Hiseq Sequencing- 5 GB Test
Short Name: 2x150 Hiseq Sequencing
Also known as: Illumina Hiseq Sequencing, High-Throughput DNA Sequencing, NGS 5GB
2x150 Hiseq Sequencing- 5 GB Test test available at DNA Labs India for ₹12,500. Uses Illumina Hiseq platform, Paired-end 2x150 bp sequencing on Extracted DNA samples. Results in Reports are delivered within 4 weeks from sample receipt.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of 2x150 Hiseq Sequencing is to provide high-resolution genetic data for accurate diagnosis and management of various conditions. It helps in identifying disease-causing mutations, guiding targeted therapies, assessing hereditary cancer risks, and understanding infectious disease genomes. This test is essential for personalized medicine, enabling clinicians to tailor treatments based on individual genetic profiles.
- Test Code
- 6445
- CPT Code
- 81479
- ICD Code
- Z01.89
- Price
- ₹12,500
- Sample Type
- Extracted DNA
- Result Time
- Reports are delivered within 4 weeks from sample receipt.
- Fasting Required
- No
- Method
- Illumina Hiseq platform, Paired-end 2x150 bp sequencing
Sample Collection
No special preparation required. However, if providing blood sample, inform your doctor about any medications or supplements you are taking.
Method: Blood sample or extracted DNA submission
Laboratory Analysis
A blood sample will be collected by a trained phlebotomist. If you are submitting extracted DNA, ensure it is properly labeled and stored.
Report Delivery
No specific aftercare required. You can resume normal activities immediately.
Timeline: Reports are delivered within 4 weeks from sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of 2x150 Hiseq Sequencing is to provide high-resolution genetic data for accurate diagnosis and management of various conditions. It helps in identifying disease-causing mutations, guiding targeted therapies, assessing hereditary cancer risks, and understanding infectious disease genomes. This test is essential for personalized medicine, enabling clinicians to tailor treatments based on individual genetic profiles.
How to Prepare
- For blood sample: Use EDTA vacutainer.
- For extracted DNA: Provide at least 1-2 µg of high-quality DNA in a sterile tube.
- Label the sample with patient name and unique ID.
- Maintain cold chain during transport if required.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"2x150 Hiseq Sequencing provides high-resolution genetic data essential for identifying clinically actionable variants. This test is particularly valuable for hereditary cancer risk assessment, rare genetic disorders, and pharmacogenomics, enabling personalized treatment strategies."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed blood sample
- Insufficient DNA quantity (<0.5 µg)
- Degraded DNA (e.g., high fragmentation)
- Improper labeling or missing requisition form
Understanding Your Results
Pathogenic
Clinical action: Confirms diagnosis; guide treatment and family screening
Likely Pathogenic
Clinical action: Consider additional evidence; may guide management
Variant of Uncertain Significance (VUS)
Clinical action: Further testing or family studies may be needed
Benign/Likely Benign
Clinical action: No clinical action required
Consult your physician or genetic counselor if you have a family history of genetic disorders, have been diagnosed with cancer, or if you are considering reproductive planning. Also, consult if you have unexplained symptoms that may have a genetic basis.
Limitations
- ⚠May not detect large structural variants or repeat expansions
- ⚠Limited to regions covered by the sequencing design
- ⚠Interpretation may require additional confirmatory testing
- ⚠Not a whole-genome sequencing service
Risks & Considerations
- ●Minimal risk of bruising or infection at blood draw site
- ●Psychological impact of genetic findings
- ●Potential for incidental findings
Interfering Factors
- ●Low DNA quality or quantity
- ●Contamination with non-human DNA
- ●PCR duplicates
- ●Insufficient sequencing depth
- ●Bioinformatics pipeline variations
Compare With Similar Tests
| Test | 2x150 Hiseq Sequencing- 5 GB | Whole Exome Sequencing (WES) | Sanger Sequencing | Whole Genome Sequencing (WGS) |
|---|---|---|---|---|
| Comparison | 2x150 Hiseq Sequencing- 5 GB |
Frequently Asked Questions
What is 2x150 Hiseq Sequencing?
What is the cost of the test?
What sample is required?
How long does it take to get results?
Is home sample collection available?
What conditions can this test help diagnose?
Do I need to fast before the test?
Can this test detect all genetic mutations?
Is the test NABL accredited?
How should I prepare for the test?
Will I get a genetic counseling session?
Can I use this test for research purposes?
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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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