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Sequencing service

2x150 Hiseq Sequencing- 1 GB

Reviewed for accuracy
₹2,500
Per sample
final quote on confirmation
Reports are typically delivered wi...
Turnaround
from sample receipt
Extracted DNA
Sample
input material
Enquiry
How to order
no payment online

Overview

The 2x150 HiSeq Sequencing (1GB) service at DNA Labs India is a high-throughput next-generation sequencing (NGS) solution designed for accurate genetic analysis. This method sequences DNA fragments of 150 base pairs from both ends (paired-end), producing 150 base pair reads in each direction. This dual-read approach enhances accuracy and reduces sequencing errors, making it ideal for detecting genetic variants, mutations, and structural changes. The service is priced affordably at INR 2500, making advanced genomic testing accessible to a broader population. It is particularly useful for diagnosing genetic disorders, identifying mutations associated with diseases, and guiding personalized treatment plans. With a turnaround time of 4 weeks, this test provides comprehensive data that can be used in clinical research, oncology, and inherited disease diagnosis. DNA Labs India ensures high-quality results with strict quality control and expert bioinformatics analysis. The test requires extracted DNA as the sample, and free home sample collection is available across major cities in India.

To be completed — reclassified from Tests on 2026-11-13.

The purpose of the 2x150 HiSeq Sequencing (1GB) test is to provide high-resolution genetic data for the diagnosis and management of genetic conditions. It is used to identify disease-causing mutations, confirm clinical diagnoses, assess genetic predispositions, and guide targeted therapies. The paired-end sequencing approach enhances the detection of insertions, deletions, and structural variants, which are often missed by other methods. This test is valuable for patients with unexplained symptoms that may have a genetic basis, as well as for research purposes.

Sample requirements

What to send us

Sample type: Extracted DNA
Volume: 1 µg (minimum)
Container: Eppendorf tube (DNA)
Collection: Blood or saliva sample for DNA extraction

Deliverables & turnaround

What you receive

Turnaround: Reports are typically delivered within 4 weeks from the date of sample receipt.

Pricing

Transparent pricing

OptionTurnaroundPrice (INR)Unit
StandardReports are typically delivered within 4...₹2,500per sample

Limitations & precautions

What this service cannot do

Detects only variants in the sequenced regions; does not cover all genomic regions
May miss large structural variants or repeat expansions
Requires high-quality DNA; degraded samples may fail
Interpretation may be limited by incomplete reference databases
Not a diagnostic test for all genetic conditions; clinical correlation required

Questions customers ask

Frequently asked questions

What is 2x150 HiSeq Sequencing?

2x150 HiSeq Sequencing is a next-generation sequencing method that reads DNA fragments of 150 base pairs from both ends, producing paired-end reads. This enhances accuracy and is used for various genetic analyses.

What is the cost of the 2x150 HiSeq Sequencing (1GB) test?

The cost is INR 2500, which is a special discounted price offered by DNA Labs India.

What sample is required for this test?

The test requires extracted DNA. DNA can be extracted from blood or saliva samples.

How long does it take to get results?

The turnaround time is 4 weeks from the date of sample receipt.

Is home sample collection available?

Yes, we offer free home sample collection for online bookings across many cities in India.

What is the difference between 1GB and other sequencing data sizes?

1GB refers to the amount of sequencing data generated. Larger data sizes provide more coverage but at a higher cost. 1GB is suitable for targeted or small-scale sequencing.

Can this test detect all genetic disorders?

No, it can detect variants in the sequenced regions. It may not cover all genomic areas, and some disorders may require other testing methods.

Is fasting required before the test?

No, fasting is not required for this test.

Will I get a report explaining the results?

Yes, you will receive a detailed report with variant classification and clinical significance, along with recommendations.

Is the test covered by insurance?

Insurance coverage is not guaranteed. You may check with your insurance provider for reimbursement options.

What is the accuracy of this sequencing method?

The error rate is less than 0.1%, and Q30 scores are typically above 80%, indicating high accuracy.

Can I use this test for pharmacogenetic testing?

Yes, the data can be used to identify genetic variants that affect drug metabolism and response.


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Editorial accountability

Written by: Diptesh Goswami, Medical Content Writer
Reviewed by: Dr Pasupathy Arumugam , Consultant Pathologist
Last updated: 07 Sep 2026

DNA Labs India

Address: 2nd Floor, Prashanthi Arcade, 202, Amberpet Main Rd, Amberpet, Hyderabad - 500013, Telangana, India

Phone:+919395142800

Enquiries are answered by our laboratory team. No payment is collected on this website.

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