Configure, Customize, and Save Your Ideal Interface
Most genomic analysis tools lock you into a fixed interface that can't be customized to your workflow.
AIVA takes a different approach: your analysis, your interface.
Design your ideal analysis interface. Show only the annotations you care about. Whether you work with 10 or 100 specialized annotations, AIVA adapts to how you think, not the other way around.
Customized Analysis Panel to Review Variant Annotations
Not all cases/samples are equal. AIVA helps you customize the analysis panel based on what annotations are important for analyzing each case.
Intelligent Variant Grouping
AIVA categorizes annotations into groups based on the type of annotation using our AI agent, for better organization and analysis. This allows you to focus on these groups (i.e. cards) that matter for your analysis and hide the rest.
Draggable Category Cards & Layout Presets
Arrange category cards intuitively by dragging them across the analysis panel. These can be moved, expanded and collapsed to focus on what matters most. Save your preferred category layouts as presets for consistent analysis across samples.
Customized Analysis Panel
Other annotations that we provide
Within your analysis panel, access powerful clinical annotations that we provide:
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Protein Structure Visualization
3D protein structure viewer integrated directly into the interface. Visualize variant positions in their full protein context. Identify variants in critical domains, binding sites, or catalytic regions without switching tools. Understand structural impact of variants by seeing exactly where amino acid changes occur in the folded protein.
Protein Structure Visualization
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ACMG Classification with Evidence Tracking
Full ACMG/AMP guideline implementation with structured evidence tracking for each criterion based on phenotype. Our agent does the classification automatically, which you can modify as needed. Export classifications directly into clinical reports.
ACMG Classification with Evidence Tracking
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Gene Level Annotations
Our inhouse knowledge base connects genes to disease associations, pathway and biological function data provide context, drug-gene interactions for pharmacogenomics, giving you a complete picture of clinical relevance.
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Team Collaborative Analysis
Teams can flag variants, add comments, and respond to comments for collaborative analysis. Complete comment history with timestamps provides an audit trail for clinical decision-making. Users can also make comments visible across samples/projects or even make them public to help other researchers.
Experience AIVA's Performance
See how AIVA handles your largest datasets with ease.
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