0.9

Initial Windows-only release.

Basic Features:

• Visualization of SVs in a multi-sample VCF file for up to approximately 60 samples in view (before scrolling is required).
• Allele frequency track.
• Gene annotation visualization.
• Supports diploid and polyploid samples.
• Supports phased and unphased SVs.
• 'Select' region(s) for comparative analyses by dragging within the coordinate system. Multiple selections must be within the same chromosome.
• Click on an SV or gene to show its information (ID, start position, etc.) in a pop-out side panel.
• Alternate colorblind-friendly theme for SVs.

Comparative Features:

• Sample track pinning
• 'Show Same Calls' - render SVs that are present in at least one pinned sample.
• 'Show Diff Calls' - render SVs that are absent in all pinned samples.
• 'Color by Haplotype' - Visualize the different patterns of SVs across samples through haplotypes based on the presence or absence of SVs.

Known Issues:
This is a highly-tested, working release, however, there are minor features and interactions that should be included/fixed in the future.

• Restoring SVs after applying 'Show Same Calls' and 'Show Diff Calls' can be achieved by zooming in/out, or if necessary, reloading the chromosome. A 'Restore' button should be included in the future.
• Scaling the track height or zooming in/out after applying Color by Haplotype will not update appropriately.