SnapGene Version 4.3.7

SnapGene 4.3.7 was released on April 17, 2019.

New Functionality

• Added support for importing Vector NTI® Express databases.
  (Requested by Takashi Watanabe and Kim Williams)
• Enhanced the import of Vector NTI® Advance databases to retain the folder structure, generate a collection, and use an improved default collection name.

Enhancements

• Added various MilliporeSigma DNA markers.
  (Requested by Emily Hilbourne)
• Added a context menu to the blank area of the aligned sequences panel when aligning to a reference DNA sequence.
  (Requested by Tobias Abel)
• Enabled Enzymes view to be more compressible horizontally.
• Improved the expected mass calculations in the agarose gel dialog.
• Improved the look and feel of small-font view tabs in dialogs on macOS.
• Changed "Sigma-Aldrich" to "MilliporeSigma".
• Changed "TransBionovo" to "TransGen Biotech".
• Made other minor textual enhancements.

Fixes

• Stabilized embedded aligned sequences when editing the reference DNA sequence and saving.
  (Reported by Jaeyoun Kim)
• Fixed a regression that could prevent circular topology detection when creating new DNA files.
  (Reported by Will Arnold)
• Ensured that map labels are always shown.
• Ensured that the number of selected files in a collection is always shown.
• Prevented a crash when selecting a profile in the multiple alignment viewer.
• Fixed an issue in which "?" characters were sometimes shown in gel lanes when no template was loaded.
• Added missing short fragments for some pBR322 MW markers.
• Ensured that a space can be entered in a contig name or at the end of a new file name on Windows if the file extension has been manually removed.
• Ensured that template menus in dialogs always update to reflect the current names of open files.
• Improved the Vector NTI® Advance database importer to tolerate Unicode characters as well as multiple files with names that differ only in case.
• Ensured that nonexisting or unmounted remote collections are removed from the "Open Recents" list.
• Fixed the Collection Overview file total counts to exclude folders.
• Ensured that a collection does not overwrite another file on a case-insensitive file system when renaming to a name that differs only in case.
• Improved the opening of older CLC Bio files.
• Fixed an issue that prevented "Hide Selected Bases" from always working.
• Ensured that when loading and viewing an alignment with a reference DNA sequence, aligned sequences are always trimmed properly.