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DNA Labs India

2x150 Hiseq Sequencing- 5 GB Test

DNA Labs India | ISO 9001:2015 Certified

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.

Next-Generation Sequencing (NGS)🏠 Home Collection

🩺 Medically Reviewed By

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
Step 1

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

Step 2

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.

Step 3

Report Delivery

No specific aftercare required. You can resume normal activities immediately.

Timeline: Reports are delivered within 4 weeks from sample receipt.

Patient Instructions

1
Before the Test:No special preparation is required. However, ensure you have a valid prescription or referral from a physician, if applicable.
2
During the Test:The test involves providing a blood sample or extracted DNA. The process is quick and minimally invasive.
3
After the Test:You can resume normal activities. Results will be available in approximately 4 weeks.

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 — 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 TypeExtracted DNA
Sample Volume1-2 µg (as per protocol)
ContainerDNA storage tube (provided by lab)
Collection MethodBlood sample or extracted DNA submission

Sample Stability

Blood: 2-8°C for up to 72 hours
Extracted DNA: -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed blood sample
  • Insufficient DNA quantity (<0.5 µg)
  • Degraded DNA (e.g., high fragmentation)
  • Improper labeling or missing requisition form

Understanding Your Results

The sequencing results are interpreted by clinical geneticists and bioinformaticians. Variants are classified according to ACMG guidelines. The report includes a list of clinically significant variants, their pathogenicity, and implications for diagnosis and treatment.
📊

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

⚠️ When to Consult a Doctor:

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

Test2x150 Hiseq Sequencing- 5 GBWhole Exome Sequencing (WES)Sanger SequencingWhole Genome Sequencing (WGS)
Comparison2x150 Hiseq Sequencing- 5 GB

Frequently Asked Questions

What is 2x150 Hiseq Sequencing?
It is a next-generation sequencing method using the Illumina Hiseq platform, producing 150 base pair reads from both ends of DNA fragments, generating 5 GB of data per sample.
What is the cost of the test?
The test costs INR 12,500 for 5 GB of data, including sample preparation, sequencing, and data analysis.
What sample is required?
Extracted DNA is required. If you don't have extracted DNA, a blood sample can be collected for DNA extraction.
How long does it take to get results?
Reports are typically delivered within 4 weeks from sample receipt.
Is home sample collection available?
Yes, we offer free home sample collection for online bookings across major cities in India.
What conditions can this test help diagnose?
It can help diagnose genetic disorders, cancer (somatic mutations), infectious diseases, and guide pharmacogenomic decisions.
Do I need to fast before the test?
No, fasting is not required for this test.
Can this test detect all genetic mutations?
No, it detects variants in the regions covered by the sequencing design. Large structural variants or repeat expansions may not be detected.
Is the test NABL accredited?
Yes, DNA Labs India is NABL accredited and follows stringent quality standards.
How should I prepare for the test?
No special preparation is needed. Inform your doctor about any medications you are taking.
Will I get a genetic counseling session?
Our reports include interpretation, and we recommend consulting with a genetic counselor or your physician for detailed discussion.
Can I use this test for research purposes?
Yes, this service can be used for research applications requiring high-throughput sequencing.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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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.

LIMS Integration

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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