Upload Data
Upload your VCF or CSV files to begin genomic analysis
Drop files here or click to upload
Supports VCF and CSV formats only
Data Preview
| Chromosome | Position | Ref | Alt | Gene | Effect |
|---|---|---|---|---|---|
| 1 | 123456 | A | G | BRCA1 | Missense |
| 2 | 789012 | C | T | TP53 | Nonsense |
Advanced Lab Setup
Professional genomics laboratory environment
Team Collaboration
Multi-disciplinary analysis team at work
Research Facility
State-of-the-art sequencing lab
Dashboard
Comprehensive genomic variant analysis
SNP vs INDEL Distribution
Chromosome Variant Distribution
Gene Impact Heatmap
Advanced Technology
Cutting-edge genomics equipment
Neon Laboratory
Modern research environment
Interactive Controls
Gesture-based data manipulation
Gene Insights
Comprehensive gene-level analysis and clinical annotations
Filters
Top Disease-Associated Genes
High RiskHigh-Risk Variants
WarningClinical Relevance
ActionableGene Variant Burden
| Gene | Chromosome | Variants | Pathogenic | Clinical Significance |
|---|---|---|---|---|
| BRCA1 | 17 | 247 | 89 | High (Breast & Ovarian Cancer) |
| TP53 | 17 | 189 | 76 | High (Li-Fraumeni Syndrome) |
| EGFR | 7 | 156 | 45 | High (Lung Cancer) |
| APC | 5 | 134 | 67 | High (Colorectal Cancer) |
| KRAS | 12 | 98 | 34 | High (Multiple Cancers) |
Advanced Lab Environment
State-of-the-art genomics facility
Research Environment
Controlled experimental conditions
Microscopy Station
High-resolution imaging capabilities
Variant Explorer
Search and analyze specific genomic variants
BRCA1:c.5266dupC
chr17:41276045 - Pathogenic
TP53:c.215C>G
chr17:7577539 - Pathogenic
APC:c.3920T>A
chr5:112175951 - VUS
MLH1:c.677G>A
chr3:37035080 - Benign
Filter Variants
Variant Details
Genomic Location
chr17:41276045
Variant Type
Insertion
Gene
BRCA1
Protein Change
p.Gln1756Profs*74
Clinical Significance
Pathogenic
Population Frequency
< 0.001%
Reports
Generate professional genomic analysis reports
Report Configuration
Preview Report
Executive Summary
Total variants analyzed: 24,567
Key Findings
3 pathogenic variants detected requiring follow-up
Clinical Significance
BRCA1 and TP53 variants associated with increased cancer risk
Download Options
Settings & Information
Platform Information
About GenomeVista
Advanced NGS variant analysis platform designed for research professionals.
Version
2.1.0 (Beta)
Last Updated
December 2024
Display Settings
Research Environment
Tech Infrastructure
Custom Setup
About the Platform
GenomeVista is a cutting-edge genomic analysis platform designed to transform raw NGS variant data into clinically actionable insights. Built with advanced algorithms and interactive visualizations, it empowers researchers to make data-driven decisions faster.
Our mission is to accelerate genomic research by making complex variant analysis accessible, accurate, and visually intuitive for the scientific community.
Privacy Policy
• All uploaded genomic data is processed locally and never stored permanently
• End-to-end encryption for all data transmissions
• No sharing of identifiable information with third parties
• Full data deletion within 24 hours of session completion
Terms of Use
• Research use only - not for diagnostic purposes
• Users retain ownership of their genomic data
• Platform provided as-is without warranties
• Compliance with institutional review boards required