Genome Intelligence Suite
Understand genomic complexity
through coordinated intelligence.
FantomX combines sequence analysis, variant interpretation, evidence synthesis, pathway modeling, and auditable agent collaboration in one secure research environment.
Interactive Explorer
Synthetic genome visualization.
Explore a demonstration chromosome structure with synthetic variant markers. All data shown is illustrative and not derived from real patient sequences.
SYNTHETIC DEMONSTRATION DATA — Not derived from real patient sequences
Research Decision Support
All genome intelligence features are designed as research and decision-support tools. They do not independently diagnose patients, authorize treatments, or replace qualified expert review. All outputs require review by appropriately qualified professionals.
Capabilities
Ten coordinated intelligence modules.
Sequence & Variant Ingestion
Securely ingest approved genomic data with format validation and provenance tracking.
Annotation Workspace
Annotate variants against reference databases with automated quality scoring.
Mutation-Impact Modeling
Model potential consequences of genetic variants using in-silico computational approaches.
Pathway & Phenotype Mapping
Map affected biological pathways and associated phenotype relationships.
CRISPR Research Simulation
Evaluate editing strategies with off-target screening and uncertainty documentation.
Comparative Scenario Analysis
Compare alternative research strategies with evidence-based scoring.
Evidence Graphs
Visualize how conclusions connect to supporting data, publications, and confidence levels.
Expert-Review Workflow
Route all outputs for qualified human review with structured approval gates.
Secure Data Controls
Encryption, residency controls, consent tagging, and access auditing.
Reproducible Export Packages
Generate versioned, reproducible analysis packages with full methodology documentation.