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Trusted Clinical Genomics Infrastructure

Smart Genome combines clinical whole genome reporting, genomic interpretation, and large-scale genome exploration in a unified platform for healthcare, research, and precision medicine.

Built on years of clinical reporting experience and validated genomic methodologies, Simplify Genomics helps organizations transform genomic data into clinically meaningful insights and actionable knowledge.

Alzheimer’s Disease Risk
Expanded Pharmacogenomics
New Health and Wellness Insights

Clinical Genomics Infrastructure

Simplify Genomics combines clinical reporting expertise, curated genomic knowledge, and scalable genomic infrastructure to support healthcare, research, and precision medicine programs.

  • CLIA-certified and CAP-accredited genomic reporting
  • Clinical Whole Genome reporting since 2018
  • Hereditary Disease, Polygenic Risk, Pharmacogenomics, and Health and Wellness Trait reporting
  • Clinical Decision Support with Genetic Counselor services

Built on genomic infrastructure originally developed at Human Longevity, Inc. and more than eight years of clinical whole-genome reporting experience.

Featured Resources

Genomic 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.

1.6M+ variants interpreted

2000+ genes and 2100+ hereditary disease associations curated

CLIA-certified and CAP-accredited Whole Genome Sequence reporting since 2018

~1.5 Billion queryable variant records