Healthcare - Breakthrough Genomics

Virtual Geneticist®, Equipping Healthcare Systems

to better utilize
genomic data

Virtual Geneticist is a modular genomic interpretation platform that enables Healthcare Systems to meet the growing demand for genetic testing and precision medicine initiatives.

Enabling Staff to Navigate Genetic
Testing with Confidence

Medical Directors

For medical directors and geneticists, Virtual Geneticist offers a cutting-edge solution to help resolve complex and unsolved cases. The platform also provides multi-factorial scoring, transparent reasoning, and detailed literature review for every variant that reduces the need for additional review time and minimizes the uncertainty around rare and VUS variants.

Clinical Operations

For clinical operations, Virtual Geneticist provides a powerful tool that helps reduce testing backlogs while improving the internal interpretation capabilities for initiatives like newborn screening and cardiovascular risk assessment. The platform also provides structured, ready-to-use outputs and audit-ready documentation for clinical staff and counselors to deliver a standardized approach to genomic testing services and care.

Genetic Counselors

Virtual Geneticist empowers genetic counselors with interpreted literature summaries that accelerate case preparation and improve communications with patients and families. The platform’s updated ACMG classifications and clear evidence presentations take the guess work out of evaluating difficult cases and helps reduce the tedious review of variant literature and the gathering of evidence from disparate sources.

Bioinformatics

For bio-informatic teams, Virtual Geneticist offers seamless integration through easy-to-deploy APIs and scales automatically as test volumes and clinical use grows. The platform also stays up to date with the latest ACMG classification guidelines, scientific publications, and evolving genomic data inputs and requirements.

As genetic testing moves from specialty centers into mainstream care, healthcare systems face the challenge of translating complex variant data into timely clinical decisions — all while managing rising patient volumes, constrained specialist resources, and aging bio-informatic infrastructure.

Offering Healthcare Systems Powerful Capabilities to Support their Precision Medicine Initiatives

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.

Reduce Interpretation Burden

Virtual Geneticist comes fully-integrated with an interpreted literature database and automated ACMG classification system that significantly reduces the manual burden of variant review while also giving users control over each evaluation.

Scale-up Test Offerings

With Virtual Geneticist, multiple test types can be analyzed within a single platform including whole genome, whole exome, long-read, gene panel tests, newborn screening, and more.

Reduce Testing Backlog

Virtual Geneticist streamlines every stage of analysis so interpretation and reporting of each test is standardized with high-throughput tools and automation to reduce manual tasks and potential errors.

Support Re-analysis of Previously Unresolved Cases

Virtual Geneticist’s powerful prioritization engine and proven ability to help resolve VUS variants gives it an advantage over competing platforms and helps boost overall diagnostic yield, even for the most difficult rare disease cases.

Core Platform Capabilities

01 Consolidated Analysis of Multiple Test Types On One Platform

Virtual Geneticist is compatible with a wide array of sequencers, data types, and tests, including: WGS, WES, RNA, Long-Read, and Gene Panel Data.

02 Resolution of Complex and Previously Negative Cases

Virtual Geneticist outperforms other platforms with advanced tools to resolve difficult and previously negative cases to boost overall diagnostic yield.

03 Automated Literature Review and ACMG Classification

Virtual Geneticist includes a fully-integrated interpreted literature database with instant access to more than 15 million variant publications.The platform’s up-to-date ACMG Classification System features multi-factorial scoring, citation-backed evidence, and optional phenotype entry.
 

04 Integration from End-to-End Deployment to Optional API

Virtual Geneticist’s 4 distinct modules can be easily customized for maximum automation and be deployed within existing workflows through seamless API.

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.

Support complex cases.
Accelerate care.
Scale precision medicine
within your system.

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