SnapGene Version 5.3.2

SnapGene 5.3.2 was released on July 06, 2021.

Fixes

• Corrected an issue with showing aligned sequences as double-stranded DNA.
  (Reported by Christine Chidester, Lauren Flynn, and Clifford Dustin Rubinstein)
• Addressed an issue with folders in collections stored on network drives.
  (Reported by Stefan Kalies)
• Addressed a stability issue with viewing some primers in Sequence view.
  (Reported by Ferdinand Greiss)
• Ensured correct reporting of the number of matches when searching ssDNA sequences.
  (Reported by Jeff Sekelsky)
• Fixed a regression that prevented the display of some primer binding sites when simplified hybridizations are being shown.
  (Reported by Katjusa Brejc)
• Increased the number of primer binding sites that can be shown in Map view.
  (Requested by Jadyn Cox, Hsinho Huang, and Sara Smith)
• Fixed an issue that sometimes prevented showing the first aligned sequence when printing an alignment to a reference sequence.
  (Reported by Daiki Matsuda)
• Corrected an issue with saving aligned reads to an ssDNA sequence.
  (Reported by Daiki Matsuda)
• Improved stability when expanding sequences aligned to a reference DNA sequence.
  (Reported by Scott Brown)
• Improved stability when choosing alternative codons.
• Ensured that opened documents are always added to the recent files list.
• Fixed an issue that could prevent enzymes from being displayed in older documents in collections.
• Ensured that display options are always preserved when duplicating collection documents in a new window.
• Removed a blank cascading menu that could appear in the Edit menu when using "Save As".
• Improved stability when dragging trimming handles.
• Improved stability when using Opt-click to invoke "Close All Open Files" on macOS.
• Improved the appearance of the focus ring for comboboxes on macOS.
• Improved the mnemonic shortcut for deleting a restriction fragment on Windows.
• Improved the default filename when exporting an alignment.
• Improved colors in cloning overviews.
• Made various textual corrections.
• Prevented unnecessary scrolling when undoing sequence modifications.
• Improved stability when using short sequences aligned to a reference DNA sequence.
• Improved stability when using "Splice to Remove Introns".