version 1.2.1 beta

This releases fixes a compatibility issue with macOS 15 Sequoia, which rendered the application unusable (due to a new Apple private class using a name used by the application), fixes other bugs, and adds the following:

• If genotypes of several samples are called together for the same marker, the application performs a comparison between samples to avoid taking alleles as artifacts (adenylation).
• Better detection of peaks from the molecular ladder, by subtracting the baseline fluorescence level.
• Reduced risk of considering noise as additional peaks during allele calling.
• Slightly improved detection of crosstalk for faint peaks.
• The detailed view now shows the row displaying sample metadata (name, etc.) when samples are stacked in the same row but only one sample is shown.
• The detailed view now shows markers, bins and other labels on traces when channels are stacked in the same row but only one channel is displayed .
• When the detailed view stacks traces from different channels in the same row and a sample doesn't have fluorescence data for the channel that is shown, this is indicated to the user at the top of the row (previously, this situation was not managed, which caused display errors). Saturated regions are still shown.
• When curves from several samples are stacked, the user can right-click or force-click a curve to reveal the associated sample in the sample table.
• When a sample/genotype is highlighted (via the dedicated button or the action described above), the highlighting stays visible until the selected row(s) change(s).
• When a bin set is resized with the "Move Bin Set" mode, bin widths are preserved.
• In the table listing genotypes, the color of a marker is denoted by a round label next to the marker name.

Thorough compatibility testing needs to be continued.

Full Changelog: v1.1-beta...v1.2.1-beta.2