Variant Report Dashboard

Generate customizable variant reports for specific genes and SNPs of interest. These reports are dynamically created using Bystro's rapid query language and can be tailored for each research deployment.

How It Works

Variant reports provide focused genetic analysis on specific variants or genes that researchers want to examine. Reports are generated dynamically using Bystro's query language, allowing for rapid searching and customization based on research needs.

Available Report Types

🧬APOE Variant Summary

Comprehensive analysis of APOE genotypes with visual summaries and individual breakdowns.

What you'll see:

  • Interactive pie chart showing APOE genotype distribution
  • Detailed table with individual genotypes (e2/e2, e2/e3, e3/e3, e3/e4, e4/e4)
  • Per-person breakdown across the entire cohort

Example table:

Sample IDAPOE GenotypeRisk Category
SAMPLE_001e2/e2Highly Protective
SAMPLE_002e2/e3Protective
SAMPLE_003e3/e3Normal
SAMPLE_004e3/e4Moderate
SAMPLE_005e4/e4Higher

📋IBD Variant Report

Focused analysis of inflammatory bowel disease-associated SNPs that researchers want to examine.

What you'll see:

  • List of top IBD-associated SNPs selected by researchers
  • Per-individual genotype status for each SNP
  • Customizable SNP selection based on research focus

Example output format:

Sample IDrs11209026rs2241880rs10995271
SAMPLE_001AAGGCT
SAMPLE_002AGAGCC
SAMPLE_003GGAATT

Customization Options

Variant reports are highly customizable and can be tailored to specific research needs using Bystro's powerful query language.

Query Language Integration

Reports are generated using Bystro's rapid query language, allowing researchers to specify exactly which variants and individuals to include.

Benefit: Fast, flexible data extraction tailored to research questions

Deployment-Specific Configuration

Each research deployment can have different variant reports configured based on the study's focus and research priorities.

Examples: Cancer studies might focus on tumor suppressor genes, cardiovascular studies on lipid metabolism variants

Researcher-Defined SNP Lists

Researchers can specify which SNPs or genes are most relevant to their study, creating focused variant reports.

Flexibility: Add, remove, or modify variant lists based on evolving research needs

Technical Implementation

Rapid Data Processing

  • Query Language: Custom syntax for rapid genetic data searching
  • Dynamic Generation: Reports created on-demand based on current data
  • Scalable Architecture: Handles large cohorts efficiently

Output Formats

  • Interactive Tables: Sortable, filterable data views
  • Visual Charts: Pie charts, bar graphs for distribution summaries
  • Exportable Data: Download results for further analysis

Getting Started

  1. 1Select Report Type: Choose from available variant reports (APOE, IBD, or custom)
  2. 2Configure Parameters: Specify cohort, filters, or additional variants if applicable
  3. 3Generate Report: Click to create the dynamic summary using rapid query processing
  4. 4Review Results: Examine tables, charts, and individual-level data