Overview
Vertebrate genome de novo assembly and annotation is a comprehensive genomics service that involves reconstructing the complete genome sequence of a vertebrate species without a reference genome. This process uses high-throughput Illumina sequencing to generate millions of short reads, which are then assembled into contiguous sequences (contigs) and scaffolds. The assembled genome is subsequently annotated to identify genes, regulatory elements, and other functional elements. This service is crucial for understanding the genetic basis of diseases, evolutionary biology, and conservation genetics. At DNA Labs India, we provide end-to-end solutions including sequencing, assembly, annotation, and bioinformatics analysis, ensuring high-quality results for research and clinical applications. Our expert team ensures rigorous quality control at every step, from sample processing to final data delivery, making this service ideal for academic institutions, research organizations, and clinical diagnostic laboratories.
To be completed — reclassified from Tests on 2026-11-13.
The purpose of vertebrate genome de novo assembly and annotation is to generate a complete and accurate reference genome for a species, enabling the identification of genetic variants, gene structures, and functional elements. This information is essential for studying disease mechanisms, developing diagnostic markers, and guiding therapeutic strategies. It also supports comparative genomics and evolutionary studies.
Sample requirements
What to send us
Deliverables & turnaround
What you receive
Turnaround: Results are typically available within 8 weeks after sample receipt.
Pricing
Transparent pricing
| Option | Turnaround | Price (INR) | Unit |
|---|---|---|---|
| Standard | Results are typically available within 8... | ₹250,000 | per sample |
Limitations & precautions
What this service cannot do
Questions customers ask
Frequently asked questions
What is vertebrate genome de novo assembly?
It is the process of reconstructing a complete genome sequence of a vertebrate species without a reference genome, using high-throughput sequencing data.
What is the cost of this test?
The cost is INR 250,000, which includes sequencing, assembly, annotation, and data analysis.
What sample type is required?
Extracted DNA is required, typically from blood or tissue samples.
How long does it take to get results?
Results are available within 8 weeks after sample receipt.
Is home sample collection available?
Yes, we offer free home sample collection for online bookings across India.
What is Illumina technology?
Illumina is a high-throughput sequencing platform known for accuracy and cost-effectiveness, widely used for genome sequencing.
What is the turnaround time?
The turnaround time is 8 weeks.
Can this test be used for clinical diagnosis?
Yes, it can help identify genetic mutations associated with diseases, but should be interpreted by a geneticist.
What is the difference between de novo assembly and resequencing?
De novo assembly builds a genome without a reference, while resequencing aligns reads to an existing reference genome.
What is genome annotation?
Genome annotation is the process of identifying genes and other functional elements in the assembled genome.
Is this test covered by insurance?
Generally not covered; please check with your insurance provider.
What quality metrics are provided?
We provide N50, BUSCO completeness, gene count, and other assembly quality metrics.
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