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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.

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Our Findings

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.