Home » Release Notes » 5.3.2

Changes in version 5.3.2 (Jul 7, 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".