2x150 Hiseq Sequencing- 10 GB Test
Short Name: 2x150 Hiseq Sequencing
Also known as: NGS Sequencing, High-Throughput Sequencing, 2x150 Paired-End Sequencing
2x150 Hiseq Sequencing- 10 GB Test test available at DNA Labs India for ₹25,000. Uses Next-Generation Sequencing (NGS), Illumina HiSeq 2x150 paired-end on DNA (extracted) samples. Results in Results are typically available within 4 weeks from the date of 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 comprehensive genetic data for the diagnosis of genetic disorders, identification of disease-causing mutations, and support for personalized medicine. It is used to detect chromosomal abnormalities, genetic mutations, inherited diseases, and cancer-related genomic alterations. This sequencing service enables researchers and clinicians to understand the genetic basis of diseases, facilitating targeted therapies and informed genetic counseling.
- Test Code
- 6444
- CPT Code
- 81479
- ICD Code
- Z01.89
- Price
- ₹25,000
- Sample Type
- DNA (extracted)
- Result Time
- Results are typically available within 4 weeks from the date of sample receipt.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS), Illumina HiSeq 2x150 paired-end
Sample Collection
No special preparation required. However, if providing blood sample, no fasting is needed.
Method: Blood or extracted DNA
Laboratory Analysis
A blood sample is collected by a trained phlebotomist. For extracted DNA, the sample is provided in a sterile tube.
Report Delivery
The sample is transported to the laboratory under controlled conditions. Results are typically available within 4 weeks.
Timeline: Results are typically available within 4 weeks from the date of sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of 2x150 Hiseq Sequencing is to provide comprehensive genetic data for the diagnosis of genetic disorders, identification of disease-causing mutations, and support for personalized medicine. It is used to detect chromosomal abnormalities, genetic mutations, inherited diseases, and cancer-related genomic alterations. This sequencing service enables researchers and clinicians to understand the genetic basis of diseases, facilitating targeted therapies and informed genetic counseling.
How to Prepare
- Ensure the sample is labeled correctly with patient ID
- Use EDTA tube for blood collection
- For DNA, use a sterile, DNase-free tube
- Avoid repeated freeze-thaw cycles
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This sequencing service provides high-depth coverage suitable for detecting variants in targeted regions, aiding in precise genetic diagnosis."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed blood samples
- Insufficient DNA quantity (<0.5 µg)
- Improperly labeled samples
- Samples received after prolonged storage
Understanding Your Results
Indicates a disease-causing mutation; clinical correlation required
High likelihood of pathogenicity; further evidence may be needed
Insufficient evidence to determine pathogenicity; may require family studies
No disease association; considered normal
Consult a genetic counselor or physician if the test reveals a pathogenic variant or if you have a family history of genetic disorders. Also, if you have symptoms suggestive of a genetic condition, seek medical advice.
Limitations
- ⚠May not detect large structural variants or repeat expansions
- ⚠Coverage depth may be insufficient for certain regions
- ⚠Bioinformatics analysis required for interpretation
- ⚠Not a diagnostic test for all genetic conditions
Risks & Considerations
- ●Minimal risk of bruising or infection at the blood draw site
- ●No significant risks associated with the sequencing procedure itself
Interfering Factors
- ●Degraded DNA samples may reduce sequencing quality
- ●Contamination with foreign DNA
- ●Insufficient DNA quantity
- ●PCR duplicates affecting variant calling
Compare With Similar Tests
| Test | 2x150 Hiseq Sequencing- 10 GB | Whole Exome Sequencing | Targeted Gene Panel |
|---|---|---|---|
| Comparison | 2x150 Hiseq Sequencing- 10 GB |
Frequently Asked Questions
What is 2x150 Hiseq Sequencing?
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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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