Empower Precision Medicine with Smart GenomeTM
Simplify Genomics empowers clinical decisions with genomic reporting and genome exploration at the speed of thought using our proprietary genome search engine.
1.6M+ variants interpreted and 400M+ queryable variant records
2000+ genes and 2100+ hereditary disease associations curated
5+ years CLIA-certified and CAP-accredited Whole Genome Sequence reporting
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Simplify Genomics, Inc. is a genomics technology and testing company that offers an analytical and interpretation platform to empower genomics in clinical care.
Learn how the Smart GenomeTM platform unifies genomic information in one platform and how our approach can be applied to transform patient care in your organization.