Changelog

Version history for the gnomAD Carrier Frequency Calculator.

v1.3.0 (2026-02-23)

Documentation Site

• VitePress documentation site with 17 pages (Guide, Use Cases, Reference, About)
• Playwright screenshot automation generating 14 WebP screenshots
• Unified deployment pipeline merging app and docs at custom domain
• CITATION.cff with CFF 1.2.0 standard and BibTeX entry
• Research-use-only disclaimers on docs landing page
• CI workflow for automated screenshot refresh on UI changes
• Streamlined README as slim landing page

v1.2.0 (2026-01-20)

Sharing and Mobile Optimization

• URL state sharing - share calculations via URL with encoded parameters
• Progressive Web App (PWA) - offline support, installable on desktop and mobile
• Manual variant exclusion - toggle individual variants in the variant table
• Mobile-responsive design optimization
• Search history - automatically saves recent gene searches with one-click restore

v1.1.0 (2026-01-19)

Release-Ready Features

• Variant table with detailed allele frequency display
• ClinGen gene-disease validity warnings
• Configurable variant filters (LoF HC, ClinVar P/LP, missense, star threshold)
• Export results functionality
• Text template editor with customizable sections
• Event logging for debugging
• Contextual help system
• Lighthouse accessibility and performance optimized (90+ scores)
• SEO meta tags and structured data

v1.0.0 (2026-01-19)

Initial Release

• 4-step wizard: gene search, patient status, frequency source, results
• gnomAD GraphQL integration (v4.1, v3.1.2, v2.1.1)
• Hardy-Weinberg carrier frequency calculation
• Population-specific frequency breakdown with founder effect detection
• German and English text generation
• Three text perspectives: affected individual, healthy carrier, family member
• Gender-inclusive German language options (*, :, /, traditional)
• Dark mode support (follows system preference)
• GitHub Pages deployment