Cattle Genome Sequencing and Variant Calling-30X Test
Short Name: Cattle Genome Seq 30X
Also known as: Bovine Whole Genome Sequencing, Cattle WGS 30X, Bovine Genomic Variant Analysis
Cattle Genome Sequencing and Variant Calling-30X Test test available at DNA Labs India for ₹0. Uses Next-Generation Sequencing (NGS), Whole Genome Sequencing (WGS) at 30X coverage, Bioinformatics variant calling on Extracted DNA samples. Results in Reports are delivered within 8 weeks from sample receipt.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
The primary purpose of Cattle Genome Sequencing and Variant Calling is to identify genetic mutations that cause inherited disorders in cattle. Early detection allows for timely intervention, management, and breeding decisions to prevent the spread of deleterious alleles. This test also aids in understanding the genetic basis of traits such as disease resistance, milk production, and growth, thereby supporting selective breeding programs and enhancing overall herd quality.
- Test Code
- 6343
- CPT Code
- 81410
- ICD Code
- Z13.9
- Sample Type
- Extracted DNA
- Result Time
- Reports are delivered within 8 weeks from sample receipt.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS), Whole Genome Sequencing (WGS) at 30X coverage, Bioinformatics variant calling
Sample Collection
Ensure the animal is healthy and not under recent antibiotic treatment. Collect sample using sterile techniques. Inform the lab about any known genetic conditions in the herd.
Method: Blood or tissue sample
Laboratory Analysis
Sample collection should be performed by a trained veterinarian or technician. Use appropriate anticoagulant for blood samples. Label the sample clearly with animal ID and date.
Report Delivery
Store the sample at recommended temperature and transport to the lab within 24 hours. Avoid repeated freeze-thaw cycles.
Timeline: Reports are delivered within 8 weeks from sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
The primary purpose of Cattle Genome Sequencing and Variant Calling is to identify genetic mutations that cause inherited disorders in cattle. Early detection allows for timely intervention, management, and breeding decisions to prevent the spread of deleterious alleles. This test also aids in understanding the genetic basis of traits such as disease resistance, milk production, and growth, thereby supporting selective breeding programs and enhancing overall herd quality.
How to Prepare
- Blood: Collect 5-10 ml in EDTA tube
- Tissue: Ear notch or hair follicles in sterile container
- Ensure sample is labeled with animal identification
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"Genomic testing in cattle is crucial for early detection of hereditary conditions, enabling informed breeding decisions and improved herd health."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed blood sample
- Insufficient quantity
- Sample not labeled correctly
- Sample received after prolonged delay without proper storage
Understanding Your Results
No increased risk for the tested genetic disorders. Animal is likely not a carrier.
Animal carries one copy of the mutation. It is healthy but can pass the mutation to offspring. Breeding with another carrier may produce affected calves.
Animal is affected by the disorder. Clinical management and breeding decisions should be discussed with a veterinarian.
Consult a veterinarian if the animal shows symptoms of genetic disorders or if you plan to use the results for breeding decisions. Genetic counseling is recommended for herd management.
Limitations
- ⚠Test may not detect all possible genetic variants
- ⚠Variant interpretation may require additional functional studies
- ⚠Results should be correlated with clinical findings
- ⚠Not a substitute for veterinary clinical diagnosis
Risks & Considerations
- ●No significant physical risks associated with sample collection
- ●Minor bleeding or bruising at blood collection site
- ●Stress to the animal during handling
Interfering Factors
- ●Poor quality or degraded DNA sample
- ●Contamination with foreign DNA
- ●Insufficient DNA quantity
- ●Recent blood transfusion in the animal
Compare With Similar Tests
| Test | Cattle Genome Sequencing and Variant Calling-30X | Bovine SNP Chip | Targeted Gene Panel | Whole Exome Sequencing |
|---|---|---|---|---|
| Comparison | Cattle Genome Sequencing and Variant Calling-30X |
Frequently Asked Questions
What is Cattle Genome Sequencing and Variant Calling?
What is the cost of the test?
What sample is required?
How long does it take to get results?
What genetic disorders can this test detect?
Is fasting required before sample collection?
Can this test be used for breeding decisions?
Is home sample collection available?
What is the coverage depth of sequencing?
Are the results confidential?
What is the difference between this test and a targeted gene panel?
How should I interpret the results?
Related Tests
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.
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.
Book Your Test
Enter your details and we'll connect you within 15 minutes.