CURIO | Applications
Applications to Drive Selection Insights
Breeder-friendly software solutions for common agrigenomics workflows
Cost-effective genome-wide variant discovery through low-pass sequencing combined with best-in-class imputation algorithms.
High-depth sequencing of selected genomic regions to guarantee detection of your most important markers.
Breeder-friendly bioinformatics to transition from microarray to NGS while keeping your valuable historical data.
New Marker Discovery
Discover novel genetic variants that traditional genotyping completely misses, including population-specific alleles and rare variants critical for disease resistance and adaptation. CURIO's comprehensive analysis reveals the genetic variants that actually matter for your specific breeding goals, not just what array designers selected years ago.
Impute to Higher Marker Density
Imputation transforms sparse genotyping data into dense, genome-wide variant maps that reveal the complete genetic architecture underlying your traits of interest. CURIO delivers imputation results in minutes using best-in-class algorithms, so there's no reason to stay limited by yesterday's marker selections.
Automated Integration for Scale
Scale your genomic analysis without scaling your workload. CURIO's automated integration seamlessly connects with your existing laboratory systems and databases, processing thousands of samples with minimal manual intervention so your team can focus on breeding decisions rather than data management.
Seeing is believing!
We'd love to learn more about your work and show you around the CURIO platform. Provide a few contact details below, and we will coordinate a time for a casual, informative discussion.