Transforming Genomic Workflows
GeneXplor equips researchers, geneticists, and bioinformaticians with specialized tools to accelerate variant interpretation and structural biology.
Clinical Variant Interpretation
Streamline the ACMG classification process by unifying critical data streams into a single dashboard.
Quickly determine if a rare missense variant is actually a common polymorphism in specific gnomAD geographic cohorts.
Identify conflicting assertions immediately. GeneXplor flags variants labeled "Pathogenic" in ClinVar that exceed allele frequency thresholds.
Generate highly structured, PDF-ready summaries of genetic findings, curated specifically for patient reports or tumor boards.
Structural Protein Biology
Bridge the gap between genomic mutations and physical protein structures.
View EXACTLY where a variant lands on an AlphaFold 3D model to see if it disrupts a crucial binding domain or catalytic site.
Visualize the linear peptide sequence alongside structural motifs (e.g., zinc fingers, kinase domains) sourced directly from UniProt.
Explore D3-powered networks of protein-protein interactions to understand how a single gene knockout might ripple through a cellular pathway.
Biomedical Literature Tracking
Cut through the noise of thousands of publications to find exactly what matters for your gene of interest.
Track the "Research Pulse" of any gene to see historical publication trends overlaid with key discovery milestones.
Access the latest studies, instantly filtered by relevance to specific diseases, variants, or biochemical pathways.
Leverage language models to condense decades of research into a plain-english "Gene Story" that explains the gene's primary function in human health.