2x150 Hiseq Sequencing-One Lane Test
Short Name: 2x150 Hiseq Sequencing
Also known as: HiSeq Paired-End Sequencing, 2x150 NGS, Whole Genome Sequencing Lane
2x150 Hiseq Sequencing-One Lane Test test available at DNA Labs India for ₹198,000. Uses Illumina HiSeq 2500, Paired-end 150 bp reads on Extracted DNA samples. Results in Reports are delivered within 3 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 genomic data for research and clinical diagnostics. It enables the detection of single nucleotide variants, insertions/deletions, copy number variations, and structural variants across the genome. This information is crucial for diagnosing genetic disorders, understanding cancer genomics, and identifying microbial pathogens. The high throughput and accuracy of the HiSeq platform make it suitable for large-scale projects requiring comprehensive genomic coverage.
- Test Code
- 6441
- CPT Code
- 81425
- ICD Code
- Z01.89
- Price
- ₹198,000
- Sample Type
- Extracted DNA
- Result Time
- Reports are delivered within 3 weeks from sample receipt.
- Fasting Required
- No
- Method
- Illumina HiSeq 2500, Paired-end 150 bp reads
Sample Collection
No special preparation is required. Ensure the DNA sample is extracted and stored properly. If providing blood, no fasting is needed.
Method: Blood or extracted DNA submission
Laboratory Analysis
Blood sample collection is routine. For extracted DNA, ensure proper labeling and transport conditions.
Report Delivery
No specific aftercare. The sample will be processed in the laboratory.
Timeline: Reports are delivered within 3 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 genomic data for research and clinical diagnostics. It enables the detection of single nucleotide variants, insertions/deletions, copy number variations, and structural variants across the genome. This information is crucial for diagnosing genetic disorders, understanding cancer genomics, and identifying microbial pathogens. The high throughput and accuracy of the HiSeq platform make it suitable for large-scale projects requiring comprehensive genomic coverage.
How to Prepare
- Use EDTA or citrate tube for blood collection
- For extracted DNA, use DNA LoBind tube
- Label the sample with patient ID and date
- Transport at 2-8°C if not immediate processing
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This high-throughput sequencing service is essential for comprehensive genomic analysis, enabling precise variant detection for both research and clinical applications."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed blood sample
- Insufficient DNA quantity (< 500 ng)
- DNA with A260/A280 < 1.8 or > 2.0
- Sample not labeled correctly
Understanding Your Results
Single Nucleotide Variant (SNV)
Insertion/Deletion (Indel)
Copy Number Variation (CNV)
Structural Variant (SV)
Consult a genetic counselor or physician if you have a family history of genetic disorders, are considering cancer genomic profiling, or need guidance on interpreting sequencing results.
Limitations
- ⚠Cannot detect large structural variants reliably
- ⚠May miss variants in repetitive regions
- ⚠Requires high-quality DNA; degraded samples may fail
- ⚠Bioinformatics analysis may require additional expertise
- ⚠Not a diagnostic test for all conditions; clinical correlation needed
Risks & Considerations
- ●No significant physical risks for blood collection
- ●Possible bruising at venipuncture site
- ●Psychological impact of genetic results
Interfering Factors
- ●DNA degradation or fragmentation
- ●Contamination with RNA or proteins
- ●Insufficient DNA quantity or quality
- ●PCR amplification bias
- ●Sample mix-up or labeling errors
Compare With Similar Tests
| Test | 2x150 Hiseq Sequencing-One Lane | |||
|---|---|---|---|---|
| Comparison | 2x150 Hiseq Sequencing-One Lane |
Frequently Asked Questions
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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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