Decode to Decide. We transform genomic data into actionable insights — from DNA to racetrack performance, from genotype to commercial value.
The world's most comprehensive equine genomics database: 40.15M+ variants, 400+ breeds, 49,697 causal variants, and a proprietary 102-gene NCDS model for phenotype prediction.
Building the genomic data infrastructure for the global equine industry
GenoMatrix is the world's leading equine genomics technology provider. Built on the EquCab 3.0 reference genome, we have constructed the most comprehensive equine variant database to date — covering 400+ breeds, 40.15 million+ variant positions, and 49,697 causal variants stratified by Tier A/B/C classification, along with the world's only complete equine structural variant library.
Through our proprietary NCDS v3.4 model (Neuro-Centric Differentiable System), we achieve precise genotype-to-phenotype prediction — spanning hereditary disease risk, athletic aptitude classification, and breed identification across all major equine populations worldwide.
Our Jump™ product suite covers five core domains, providing end-to-end genomics solutions for breeding farms, trading platforms, racing authorities, and government conservation programs. With 6.2 million+ horses in China alone, the market demands a genomic data infrastructure upgrade.
Every variant annotated with multi-layered evidence — VEP, SIFT, PolyPhen-2, and experimental validation. 90% core gene verification rate across 102 NCDS genes.
400+ breeds worldwide with allele frequency data. The most comprehensive coverage of Asian, European, and American equine populations in a single database.
Genomics-powered verification for equine transactions — hereditary disease risk, pedigree authenticity, and athletic potential assessment as a neutral third party.
33 specialized capabilities, 27 with undisputed global leadership — backed by data, proven by scale
The world's only equine whole-genome variant database covering SNP, Indel, and SV types, with allele frequency data across 400+ breeds.
The largest VEP (Variant Effect Predictor) annotation set for equine species, with complete transcript-level variant effect prediction coverage.
The most comprehensive dual-algorithm coverage for missense variant functional prediction — both SIFT and PolyPhen-2 scores for every variant.
Tier A/B/C stratified causal variants integrating multi-omics evidence from WGS and GWAS studies — the largest equine causal variant database globally.
The world's only complete equine structural variant database covering all five major types: deletions, insertions, inversions, duplications, and copy number variants.
A gene regulatory network of 5,178 nodes and 125,342 edges, revealing ACTIVATE, INHIBIT, and MODULATE causal relationships between genes.
Allele frequency data for 400+ equine breeds worldwide. From Thoroughbreds to Mongolian horses, Arabians to Miniature Horses — complete representation.
60,512 SNP markers in the chromosome 1 speed gene cluster, providing ultra-high resolution markers for athletic performance genetic analysis.
102-gene Neuro-Centric Differentiable System with 90% core gene validation rate. 7 athletic scoring engines powering 25 breed-specific product panels.
Five product lines covering the full equine genomics pipeline — from hereditary health to athletic performance, from identity verification to functional stratification
Whole-genome sequencing-based hereditary disease risk assessment system. Covers 8+ major hereditary diseases with Clear / Carrier / At-Risk tri-state evaluation for breeding safety decisions.
High-precision genetic identity platform built on 40.15M+ variant positions. Enables unique individual identification, parentage verification, breed purity analysis, and population diversity assessment.
Causal regulatory network and knowledge graph engine. Reveals ACTIVATE, INHIBIT, and MODULATE regulatory relationships between genes, building complete causal chains from upstream regulators to downstream phenotypes.
Athletic aptitude prediction system powered by the NCDS v3.4 Neuro-Skeletal-Developmental model. Precisely matches individuals to Sprint, Endurance, Dressage, Jumping, and Racing disciplines.
Multi-level gene functional classification system based on functional importance. From core regulatory genes to peripheral modifiers — systematic management of equine genome functional annotations and causal stratification.
From breeding farms to trading platforms, from racetracks to conservation programs — genomics-driven decision making at every critical point
Pre-breeding whole-genome screening for stallions and broodmares. Identify risks for HYPP, PSSM, and 6+ hereditary diseases to reduce breeding losses and improve offspring health outcomes.
JumpHealth™NCDS model-based prediction of athletic aptitude across sprint, endurance, dressage, and jumping disciplines. Supports training direction decisions and purchase evaluations.
JumpSport™Individual genetic fingerprinting based on 40.15M+ variant positions. Enables breed identification, parentage verification, and pedigree purity analysis with molecular evidence.
JumpID™Independent third-party genomic verification for equine transactions — hereditary health status, pedigree authenticity, and athletic potential assessment. Eliminating information asymmetry.
Full Product SuiteGenomic data support for breed conservation programs. Establishing genetic diversity baselines and informing conservation strategies for indigenous equine populations.
Data InfrastructureCausal regulatory network and phenotype prediction-powered breeding optimization. Balancing hereditary disease risk, athletic performance, and conformation traits across multiple dimensions.
JumpChain™ + JumpSport™From raw sequencing data to actionable insights — a fully proprietary analysis engine
Neuro-Centric Differentiable System — a 102-gene neuro-skeletal-developmental model. Integrating neural regulation, skeletal development, and metabolic pathway analysis for multi-layer phenotype prediction. 90% core gene validation rate.
5,178 nodes and 125,342 edges gene regulatory network with interactive force-directed graph visualization. Real-time zoom, drag, and node drill-down capabilities revealing causal regulatory relationships.
982 data tables, 41,896 gene annotations, 40.15 million variant positions. Full annotation pipeline built on the EquCab 3.0 reference genome. 22 GB complete database.
16 standardized API endpoints supporting gene queries, phenotype analysis, JumpHealth reports, athletic classification, and more. Complete Swagger documentation available.
Allele frequency data for 400+ equine breeds worldwide. From Thoroughbreds to Mongolian horses, Arabians to Miniature Horses — comprehensive representation across all major equine populations.
Every causal edge annotated with WGS/GWAS evidence sources, distinguishing experimental vs. predicted confidence levels. 49,697 causal variants managed with Tier A/B/C stratification.
GenoMatrix's hereditary disease screening has reduced our breeding losses by 40%. The JumpHealth reports are scientifically rigorous and actionable.
The NCDS athletic aptitude model's accuracy impressed us. It significantly aids our assessment of young horses' training direction and market value.
GenoMatrix is the only platform globally with comprehensive Chinese native breed genomic data. Irreplaceable for our conservation programs.
Frontier research · North America academic collaboration · Technology R&D
Global operations management · APAC client support · Compliance & certification · Technology transfer
Core R&D · Whole-genome data analysis · Database operations
From genotype to phenotype, from data to decisions.
GenoMatrix is redefining the analytical paradigm of equine genomics.
Partner with us to unlock the genomic potential of every horse.
📧 contact@genomatrix.ai · 🌐 genomatrix.ai · 📍 Shanghai, China