Pawseq™ 15X Research WGS
Population studies, breeder insights, and early-stage genomic exploration with 15X average coverage, suitable for cohort discovery.
- WGS sequencing
- Variant call file (VCF)
- Research report
- Bioinformatics access
- Researchers
- Breeders
- Institutional studies
Pawseq™ insights are intended to support preventive wellness and veterinary decision-making. They do not replace diagnosis or treatment by a licensed veterinarian.
FAQ
How accurate is Pawseq™ whole genome sequencing?
Pawseq™ uses next-generation sequencing platforms with tier-appropriate coverage (15X, 20X, 30X). 30X clinical coverage supports high-confidence variant interpretation for veterinary decision-making.
Can my veterinarian access the reports?
Yes. Pet owners can share reports with their veterinarian directly from the dashboard. Veterinary clinics on Pawseq™ receive a clinical-grade view with AI interpretation.
Do supplements require a DNA test?
No. Supplements can be ordered independently, but pairing them with a DNA insight makes recommendations more personalized.
Is my pet's genetic data secure?
Pawseq™ is designed around secure cloud architecture, permission-based data sharing, chain-of-custody sample tracking, and audit trails.
Does Pawseq™ diagnose disease?
No. Pawseq™ insights are intended to support preventive wellness and veterinary decision-making. Clinical interpretation should be reviewed with a qualified veterinary professional.
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