Virtual Geneticist Plus
End-to-End Solution
for NGS Analysis
and Reporting
Virtual Geneticist Plus offers a complete set of advanced tools for variant interpretation, secondary analysis, and clinical reporting.
The platform supports a wide range of genetic tests and data types and gives users complete variant annotation with ACMG scoring and literature backed evidence. Users get full control of every case evaluation with a sophisticated variant filtering system and time-saving reporting features.
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-Powered Filters for Fully-Customized Analysis
Comprehensive Interpretation of Complex Variants Types
Integrated Pipeline for Secondary Analysis
With Virtual Geneticist Plus, users get
access to all 4 Modules
Yearly Licenses for Virtual Geneticist Plus include access to all 4 modules including VG-Variant, Virtual Geneticist, and the AI Genetics Research Agent.
VG Variant
A scalable variant annotation and interpretation engine designed to help contextualize and resolve difficult and rare variants.
- Comprehensive literature-backed evidence
- ACMG Classification System with multi-factorial scoring, full user control, and optional phenotype entry
- API-ready architecture for seamless workflow integration
Virtual Geneticist
A genomic interpretation platform designed for rare disease diagnosis in high-throughput clinical labs, hospitals, and undiagnosed disease programs.
- Advanced variant prioritization and phenotype-driven analysis
- Automated natural language processing of clinical notes and patient phenotypes
- Parallel sample processing for scalable case analysis
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-Powered Filters for Fully-Customized Analysis
- Comprehensive Interpretation of Complex Variants Types
- Integrated Pipeline for Secondary Analysis
AI Genetics Research Agent
A genomics-focused research and translational medicine assistant for biopharma, clinical genomics, and specialty interpretation teams.
- Customizable interactive assistant for genomics-specific questions
- Literature-cited answers with clear supporting rationale
How it works
1
Upload
FASTQ,
BAM, or VCF
Files
2
Review
Quality
Control Metrics
of Underlying
Sequencing
Data
3
Search
and Filter
Prioritized
Variants
4
Evaluate
Evidence,
Literature Over-
views, and
ACMG Scoring
5
Select
Report
Template and
Variants for
Reporting"
What’s Included
Match Virtual Geneticists to Your Workflow
The platform’s secondary analysis pipeline is sequencer agnostic and compatible with a wide-range data types including short-read and long-read Whole Genome, Whole Exome, RNA, and specialty gene panels. The platform’s dynamic Quality Control Panel displays dozens of QC metrics and provides 1-click access to the Integrative Genomics Viewer (IGV) for every variant being evaluated.
Match Virtual Geneticists to Your Workflow
Virtual Geneticist Plus enables users to take full control over every analysis with an AI-driven variant filtering system to sort and prioritize potential disease-causing variants. The platform displays every variant with phenotype-driven analysis as optional. Users can also evaluate variants based on pathogenicity scores, inheritance pattern, regions of interest, allele fractions, in-silico prediction, ACMG classification, and more.
Match Virtual Geneticists to Your Workflow
Virtual Geneticist Plus accurately addresses difficult genomic regions and variant types including: CNVs, structural, trinucleotide repeats, low penetrance, intronic, complex star alleles, mitochondrial and other difficult-to-detect variant types. The platform also provides robust modules for cohort and trio analyses.
Match Virtual Geneticists to Your Workflow
Virtual Geneticist Plus creates a high-efficiency workflow for variant interpretation and clinical reporting with self-populating variant and gene information, literature references, and customizable report templates. For larger teams and institutional users, the platform also provides tiered access, audit tracking, and version control.
Use Cases
Comprehensive Analysis
for a wide range
of NGS tests
High-Performance
Interpretation for
Newborn screening
programs
Customized WGS
Interpretation for Research
and Biopharma
Actionable Reporting
for Clinical Labs
Expand capabilities to meet
the needs of the moment.
Customized Deployment Options
Cloud- hosted SaaS
Private Cloud
Region-specific deployment for data sovereignty needs
On-premise deployment for sensitive environments
3rd Party Integrations into EHR systems
Scientific Publications
Explore Virtual
Geneticist Plus
Contact Us Today
