We are the only scientifically validated genetic prediction technology for consumers. Read more
OmicsEdge Capabilities
How It Works
Upload raw genetic data to our platform or take advantage of our CLIA/CAP certified DNA test kit.
While whole genome sequencing provides a complete picture of genetic variation, its high costs make it impractical for large-scale applications. Most large genomics projects opt for genotyping arrays, which are more affordable but capture fewer variants. Here’s where Selphi comes in—our advanced imputation model transforms the limited data from genotyping arrays into a comprehensive genetic profile, delivering WGS-level insights at a fraction of the cost.
Imputation accuracy is the backbone of any genomic analysis. Selphi is designed to exceed expectations, offering unmatched precision in predicting missing genetic variants. As demonstrated in Figure 1, Selphi consistently outperforms other leading imputation methods across all allele frequencies, especially excelling with rare variants that are often crucial for identifying medically significant traits. This accuracy ensures your products can deliver high-quality, actionable insights to your customers.
Diversity matters in genomics. Selphi’s performance isn’t limited to a single population; it’s been rigorously tested and proven to deliver superior results across diverse super populations, including Africans, East and South Asians, and Europeans. This means you can trust Selphi to provide reliable and comprehensive insights, regardless of your customer base’s genetic background.
Integrating Selphi into your health tech products not only enhances the quality of your offerings but also positions your company as a leader in the rapidly evolving field of personalized medicine. Provide your customers with the most accurate, comprehensive genetic insights available—without the prohibitive costs of whole genome sequencing.
Don’t settle for genomics solutions that focus on a handful of SNPs. Enhance your products with OmicsEdge’s Selphi and empower your customers with unparalleled genomic insights.
The OmicsEdge Advantage
Discover our full suite of health reports and features in one comprehensive guide.
Our Reports & Features Summary shows all the reports, tools, and insights you can get with OmicsEdge.
We support raw DNA files with the formats .txt, .csv, .zip, and .gz.
The Dante Labs & Nebula files we accept are the SNP VCF file.
Sometimes we can support files in other formats. If you would like us to test whether your file will be compatible with SelfDecode, please email it to support@omicsedge.com and request that we try it out for you.