Genomic Intelligence for Public Health Programs

at the scale required by population-level genomics

Virtual Geneticist supports government and public health initiatives by turning genomic data into consistent, reviewable, evidence-backed insight, with the efficiencies needed for large multi-stakeholder projects. 
 


Multiplying Workforce Efficiency to Scale Genomics Expertise 

Population Health
& Precision Medicine

Virtual Geneticist’s high-throughput modules support risk identification, prevention, and longitudinal precision health strategies that population health and precision medicine programs have built their core principals on.

Newborn
Screening

For newborn screening, Virtual Geneticist provides consistent review of genomic findings in high-volume settings. the platform helps teams with up to date and consistent review and standardizes interpretation workflows adding a layer of confidence as genomic testing expands.

Cutting-Edge Genomic Research

For public health genomic research teams, Virtual Geneticist helps turn complex genomic findings into structured evidence. The platform supports variant annotation, literature review, and data synthesis so researchers can move faster from data analysis to program-relevant insight.

State & Federal Pilot Programs

For state and federal pilot programs, Virtual Geneticist provides a flexible foundation for evaluating new genomic initiatives. The platform helps teams test workflows, assess feasibility, generate structured outputs, and build the evidence needed to inform broader implementation.

As genomic testing becomes more of a priority for public health initiatives, programs face the dual challenge of building the infrastructure to analyze variants at scale while ensuring findings are accurate, accessible, and actionable across diverse communities and stakeholders.

Designed for Complex, Multi-Stakeholder
Genomic Programs 

Match Virtual Geneticists to Your Workflow

Select modular solutions to match your needs from variant annotation to full rare disease diagnosis with four purpose-built modules from single variant annotation all the way to clinical reports, newborn screening, and beyond.

Strengthen Evidence Review

Bring together up to date variant annotation, published literature, gene-disease evidence, and phenotype context into structured outputs, that are easy to review and fit into existing workflows.

Support Transparent Decision-Making

Provide citation-backed evidence and clear interpretation logic to support review, documentation, and better inform stakeholders, including key opinion leaders and policy decision makers.

Secure Integration into Existing Systems

Use modular capabilities and API-ready architecture to support clinical settings, research, informatics, and public health data environments.

Core Capabilities

01

Automated Literature Review and ACMG Classification

Facilitate genomic evidence review across defined patient or participant populations. Virtual Geneticist can help teams evaluate complex findings, organize evidence, and support population health or precision medicine initiatives.

02

Pilot and Validation Support

Support focused evaluations of genomic workflows, interpretation efficiency, evidence completeness, or implementation feasibility. Virtual Geneticist can help state, federal, and academic partners test use cases before broader deployment.

03

Cohort & Population-level analysis

Facilitate genomic evidence review across defined patients, families or participant populations. Virtual Geneticist can help teams evaluate complex variants, organize evidence, and support population health or precision medicine initiatives and research.

04

Collaborative infrastructure 

Increase the workflow efficiency of geneticists, researchers, counselors, analysts, and public health teams without removing expert judgment. Virtual Geneticist helps organize evidence and accelerate review while preserving human oversight.

Introducing the Virtual Geneticist Modules


VG Variant


A scalable variant annotation and interpretation engine designed to help contextualize and resolve difficult and rare variants.


Virtual Geneticist

A genomic interpretation platform designed for rare disease diagnosis in high-throughput clinical labs, hospitals, and undiagnosed disease programs.


Virtual Geneticist Plus

End-to-end solution for customized NGS analysis and reporting for use in clinical labs, newborn screening programs, and a variety of WGS applications.


AI Genetics Research Agent

A genomics-focused research and translational medicine assistant for biopharma, clinical genomics, and specialty interpretation teams.

Empower Precision Medicine
With Scalable Solutions.
Make a difference in
people’s lives.

Contact Us Today

“Variant Interpretation is becoming increasingly more complex, so having a tool like Virtual Geneticist allows me to quickly zero in on the correct diagnosis.”



Dr. Adrienne Elbert, MD
BC Children’s Hospital