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DNA Labs India

Cattle Genome Sequencing-30X Test

DNA Labs India | ISO 9001:2015 Certified

Cattle Genome Sequencing-30X Test

Short Name: Cattle Genome Seq 30X

Also known as: Bovine Whole Genome Sequencing, Cattle WGS 30X

Cattle Genome Sequencing-30X Test test available at DNA Labs India for ₹185,000. Uses Next-Generation Sequencing (NGS), Whole Genome Sequencing on Extracted DNA samples. Results in Results are typically available within 5 weeks from the date of sample receipt. You will be notified via email or SMS when the report is ready.. Free home collection in 300+ cities across India.

Molecular🏠 Home Collection

🩺 Medically Reviewed By

Overview

The primary purpose of cattle genome sequencing is to provide a complete genetic profile of an individual animal. This information is used to identify genetic mutations associated with inherited diseases, assess carrier status for recessive disorders, and understand the genetic basis of desirable traits such as milk production, growth rate, and disease resistance. It also aids in parentage verification and genomic selection, enabling breeders to make precise breeding decisions that enhance herd genetics over generations. Additionally, the test can reveal susceptibility to certain diseases, allowing for proactive management and preventive care. Ultimately, the goal is to improve the overall health, productivity, and profitability of cattle operations.

Test Code
6364
CPT Code
81435
ICD Code
Z13.9
Price
₹185,000
Sample Type
Extracted DNA
Result Time
Results are typically available within 5 weeks from the date of sample receipt. You will be notified via email or SMS when the report is ready.
Fasting Required
No
Method
Next-Generation Sequencing (NGS), Whole Genome Sequencing
Step 1

Sample Collection

No special preparation is required. Ensure the animal is properly restrained for sample collection. Inform the veterinarian about any medications or supplements the animal is receiving.

Method: Blood or tissue sample

Step 2

Laboratory Analysis

A blood sample is drawn from the jugular vein or a tissue sample (e.g., ear notch) is collected using a sterile technique. The sample is placed in the provided collection tube and labeled correctly.

Step 3

Report Delivery

The sample should be transported to the laboratory as soon as possible. If there is a delay, store the sample at 2-8°C for up to 72 hours. Avoid freezing the sample unless specified.

Timeline: Results are typically available within 5 weeks from the date of sample receipt. You will be notified via email or SMS when the report is ready.

Patient Instructions

1
Before the Test:No special preparation is needed. Ensure the animal is healthy and not under stress. Provide accurate animal identification and pedigree information.
2
During the Test:The sample collection is quick and minimally invasive. The animal may experience slight discomfort during blood draw.
3
After the Test:No specific aftercare is required. The animal can resume normal activities immediately.

About This Test

Who Should Get This Test

The primary purpose of cattle genome sequencing is to provide a complete genetic profile of an individual animal. This information is used to identify genetic mutations associated with inherited diseases, assess carrier status for recessive disorders, and understand the genetic basis of desirable traits such as milk production, growth rate, and disease resistance. It also aids in parentage verification and genomic selection, enabling breeders to make precise breeding decisions that enhance herd genetics over generations. Additionally, the test can reveal susceptibility to certain diseases, allowing for proactive management and preventive care. Ultimately, the goal is to improve the overall health, productivity, and profitability of cattle operations.

How to Prepare

  • Use sterile equipment to avoid contamination
  • Collect at least 2-5 µg of DNA or 2-3 ml of blood
  • Label the sample with animal ID and date
  • Transport in a leak-proof container
  • Maintain cold chain if required

Doctor's Notes

Reviewed by — MBBS, MD (General Medicine) · Reg. No. 8052

"Genomic sequencing empowers cattle breeders to make data-driven decisions, improving herd health and productivity."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeExtracted DNA
Sample Volume2-5 µg
ContainerEDTA tube or DNA stabilization tube
Collection MethodBlood or tissue sample

Sample Stability

Blood: 7 days at 2-8°C
Extracted DNA: 6 months at -20°C
Tissue: 48 hours at 2-8°C
Sample Rejection Criteria:
  • Hemolyzed blood sample
  • Insufficient quantity
  • Improper labeling
  • Sample not received in appropriate container

Understanding Your Results

The results of cattle genome sequencing are interpreted by comparing the animal's genetic variants to reference genomes and known databases. The report highlights clinically significant mutations, carrier statuses, and trait-associated markers. A geneticist or veterinarian will provide a detailed explanation and recommendations for breeding or management.
📊

Pathogenic variant in a disease-associated gene

Animal may be affected or at risk for the disorder

Recommendation: Consult veterinarian for management and breeding decisions

📊

Carrier status for a recessive disorder

Animal is healthy but can pass the mutation to offspring

Recommendation: Avoid breeding with another carrier to prevent affected offspring

📊

Presence of favorable production trait markers

Animal has genetic potential for high milk yield or growth

Recommendation: Utilize in breeding programs to enhance herd genetics

📊

No significant variants detected

No known genetic issues identified

Recommendation: Continue routine health monitoring

⚠️ When to Consult a Doctor:

If the test identifies a genetic mutation associated with a disease, or if you have concerns about your herd's health, consult a veterinarian or animal geneticist for further guidance.

Limitations

  • Results are for research and informational purposes; not a substitute for veterinary clinical diagnosis
  • May not detect all possible genetic variants due to reference genome limitations
  • Interpretation may require expert genetic counseling
  • Not intended for human diagnostic use

Risks & Considerations

  • Minimal risk of bleeding or infection at the collection site
  • Stress to the animal during handling
  • No direct health risks from the test itself

Interfering Factors

  • Poor quality or degraded DNA sample
  • Contamination with foreign DNA
  • Incomplete sample labeling
  • Insufficient DNA quantity

Compare With Similar Tests

TestCattle Genome Sequencing-30XCattle Microarray (SNP Chip)Cattle Exome SequencingCattle Whole Genome Sequencing (10X)
ComparisonCattle Genome Sequencing-30X

Frequently Asked Questions

What is cattle genome sequencing?
Cattle genome sequencing is a comprehensive genetic test that decodes the entire DNA sequence of a cow, providing insights into its health, traits, and disease risks.
Why is 30X coverage important?
30X coverage means each base of the genome is read on average 30 times, ensuring high accuracy and reliability in variant detection, which is crucial for making breeding and health decisions.
What sample is required for the test?
The test requires an extracted DNA sample, typically obtained from blood or tissue (e.g., ear notch). The sample is collected by a veterinarian or trained professional.
How long does it take to get results?
Results are available within 5 weeks from the date of sample receipt at the laboratory.
What is the cost of the test?
The cost is INR 185,000 for 30X coverage, which includes DNA extraction, library preparation, sequencing, and basic bioinformatics analysis.
Can this test identify genetic diseases?
Yes, the test can identify mutations associated with inherited diseases and carrier status for recessive disorders, helping in early diagnosis and management.
Is home sample collection available?
Yes, we offer free home sample collection for online bookings across India, including major cities like Mumbai, Delhi, Bangalore, and more.
What is the difference between 10X and 30X sequencing?
30X sequencing provides higher coverage, leading to more accurate detection of variants, especially for complex regions, compared to 10X coverage.
Can this test be used for breeding decisions?
Absolutely. The genetic information helps in selecting animals with desirable traits and avoiding carriers of harmful mutations, thereby improving herd genetics.
Are there any risks to the animal?
The test is minimally invasive. The only risks are minor bleeding or infection at the collection site, which are rare.
How should the sample be transported?
The sample should be kept at 2-8°C and transported to the lab within 72 hours. Use a leak-proof container and proper labeling.
Is the test NABL accredited?
Yes, DNA Labs India is NABL accredited and ISO certified, ensuring high-quality testing standards.
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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For Hospitals & Clinics

Reference Laboratory Services

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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