Overview
Cattle Genome Sequencing and Variant Calling is a comprehensive genomic analysis that decodes the entire DNA sequence of an individual bovine. Using advanced next-generation sequencing (NGS) technology at 10X coverage, this test identifies single nucleotide polymorphisms (SNPs), insertions/deletions (indels), and structural variants across the genome. These variants are crucial for understanding genetic traits related to disease resistance, milk production, meat quality, fertility, and adaptability to environmental conditions. At DNA Labs India, we provide a high-quality, cost-effective solution for farmers, livestock breeders, and researchers. The test begins with sample collection (blood, hair, or tissue) from which DNA is extracted. The extracted DNA undergoes whole genome sequencing, generating massive data that is analyzed using robust bioinformatics pipelines. The resulting report details clinically significant variants, their potential phenotypic impact, and recommendations for breeding or management. This information empowers stakeholders to make data-driven decisions to enhance herd health, productivity, and profitability. With a turnaround time of 8 weeks and free home sample collection across major Indian cities, DNA Labs India ensures accessibility and reliability. The test is performed in NABL-accredited laboratories with strict quality controls, ensuring accurate and reproducible results. Whether you are a dairy farmer aiming to improve milk yield, a beef producer focusing on marbling, or a researcher studying bovine genetics, this test provides the genomic insights needed to achieve your goals.
To be completed — reclassified from Tests on 2026-11-13.
The primary purpose of Cattle Genome Sequencing and Variant Calling is to provide a complete genetic blueprint of an individual animal. This enables the identification of beneficial and deleterious genetic variants that influence economically important traits. By understanding the genetic makeup, breeders can select animals with superior genetics for breeding programs, reduce the incidence of hereditary diseases, and optimize herd management strategies. The test also supports research initiatives aimed at improving cattle health and productivity.
Sample requirements
What to send us
Deliverables & turnaround
What you receive
Turnaround: Results are typically available within 8 weeks from the date of sample receipt. You will be notified via email or SMS when the report is ready.
Pricing
Transparent pricing
| Option | Turnaround | Price (INR) | Unit |
|---|---|---|---|
| Standard | Results are typically available within 8... | ₹225,000 | per sample |
Limitations & precautions
What this service cannot do
Questions customers ask
Frequently asked questions
What is the cost of Cattle Genome Sequencing and Variant Calling-10X at DNA Labs India?
The cost is INR 225,000, which includes whole genome sequencing at 10X coverage, variant calling, and a comprehensive report.
What sample types are accepted for this test?
We accept extracted DNA, blood (EDTA), hair follicles, or tissue biopsy samples.
How long does it take to get the results?
The turnaround time is 8 weeks from the date of sample receipt.
Is home sample collection available?
Yes, we offer free home sample collection for online bookings across major cities in India.
What is the difference between 10X and 30X genome sequencing?
10X coverage is more cost-effective and sufficient for most variant detection, while 30X provides higher accuracy for rare variants and structural changes.
Can this test identify all genetic diseases in cattle?
It can identify variants associated with known hereditary diseases, but not all diseases are fully understood. Some variants may be of unknown significance.
Do I need to fast the animal before sample collection?
No, fasting is not required for this test.
Will the report include recommendations for breeding?
Yes, the report includes actionable recommendations based on the genetic findings.
Is this test suitable for all cattle breeds?
Yes, the test is breed-agnostic, but variant interpretation may be influenced by breed-specific reference genomes.
How should I store the sample before shipping?
Blood should be stored at 2-8°C, hair at room temperature, and tissue at 2-8°C or frozen if shipping takes longer.
Can this test be used for research purposes?
Absolutely, it is ideal for research on bovine genomics, trait mapping, and population studies.
What is the accuracy of the variant calling?
With 10X coverage, the accuracy is high for common variants, but rare variants may require confirmation by Sanger sequencing.
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