Overview
The Vertebrate Genome Reference Based Data Analysis using Illumina technology is a comprehensive genomic test that sequences an individual vertebrate's genome and compares it to a reference genome of the same species. This high-throughput approach identifies genetic variations including single nucleotide polymorphisms (SNPs), insertions, deletions, and structural variants. The analysis provides critical insights into evolutionary relationships, population genetics, disease susceptibility, and pharmacogenomics. At DNA Labs India, this test is performed using Illumina sequencing platforms, known for their accuracy and high data output. The bioinformatics pipeline includes quality control, alignment to the reference genome, variant calling, and annotation. The resulting report highlights clinically relevant variants and their potential implications. This test is valuable for researchers, conservation biologists, and clinicians investigating genetic disorders with a vertebrate model. The cost is INR 50000, with a turnaround time of 4 weeks. Home sample collection is available across major Indian cities.
To be completed — reclassified from Tests on 2026-11-13.
The purpose of this analysis is to detect genetic variations in vertebrate genomes that may be associated with disease susceptibility, drug response, or evolutionary adaptations. It aids in understanding the genetic basis of complex traits and supports research in evolutionary biology and conservation genetics.
Sample requirements
What to send us
Deliverables & turnaround
What you receive
Turnaround: Reports are typically available within 4 weeks from the date of sample receipt.
Pricing
Transparent pricing
| Option | Turnaround | Price (INR) | Unit |
|---|---|---|---|
| Standard | Reports are typically available within 4... | ₹50,000 | per sample |
Limitations & precautions
What this service cannot do
Questions customers ask
Frequently asked questions
What is Vertebrate Genome Reference Based Data Analysis?
It is a high-throughput sequencing test that compares an individual vertebrate's genome to a reference genome to identify genetic variations such as SNPs, indels, and structural variants.
What is the cost of this test at DNA Labs India?
The cost is INR 50000, which includes bioinformatics analysis and a comprehensive report.
What sample is required for this test?
A whole blood sample (2-3 ml in EDTA) or extracted DNA (1-2 µg) is required.
Do I need to fast before the test?
No, fasting is not required for this test.
How long does it take to get the results?
The turnaround time is approximately 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 kind of genetic variations can be detected?
The test detects single nucleotide polymorphisms (SNPs), insertions/deletions (indels), structural variants, and copy number variations.
Can this test be used for disease diagnosis?
It can identify variants associated with disease susceptibility, but it is not a diagnostic test for a specific disease without clinical correlation.
Is this test suitable for research purposes?
Yes, it is widely used in evolutionary biology, population genetics, and conservation research.
What is the role of the Illumina platform in this test?
Illumina sequencing provides high accuracy and high throughput, enabling comprehensive genome coverage and reliable variant detection.
Are there any risks associated with the test?
The only risk is minimal bruising or infection at the blood draw site, which is rare.
How should I interpret the results?
Results should be interpreted by a qualified geneticist or healthcare provider, who will explain the clinical significance of any variants found.
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