The completion of the Human Genome Project was a monumental achievement, but more than 20 years later there's still a challenge navigating the vast ocean of sequencing data.
When lives are at stake, how do you ensure you're finding all the scientific and clinical evidence necessary to make an accurate diagnosis and optimal treatment decision? Enter Genomenon.
Our mission is simple: Make genomic information actionable. Our goals are clear: Empower clinicians to diagnose rare diseases in cancer, inform treatment decisions and support researchers in developing Precision medicine. Our approach is ambitious: Curating the entire human genome to understand the impact of every variant on every disease. This approach entails continuously indexing millions of full text articles and supplemental data sets containing genomic information as they're updated weekly with new evidence, normalizing genetic nomenclature across the hundreds of ways variants can be described in articles and documents. Identifying associations between variants diseases and phenotypes, connecting variants to therapies and clinical trials, employing a powerful combination of artificial intelligence and scientific experts to curate the evidence for clinical use.
The engine behind our unprecedented curation capability is two-fold. First, our genomic artificial intelligence systematically indexes the entire human genome gene by gene. Second, our team of genetic scientists curates all published evidence for every variant organizing it according to clinical guidelines to render a provisional interpretation.
The result the most comprehensive evidence-based genomic data set in the world powering clinical diagnosis and genetic research.Genomenon, making genomic information actionable to help save and improve lives. Contact us today to learn more.
