Changes in version 6.0.3 (Apr 18, 2022)

Enhancements:

• Impoved formatting when using the Copy Selected Primers and Export Primer Data commands.
  (Requested by Di Xia)
• Improved responsiveness of cloning dialogs when switching tabs and flipping fragments.
• Improved responsiveness when making selections in multiple sequence alignments.
• Improved responsiveness when performing or opening a file with an alignment to a reference sequence.

Fixes:

• Fixed an issue with renaming folders in collections.
  (Reported by Dinesh Babu Paudel)
• Avoid switching from Map to Sequence view after importing sequences to align to the reference.
  (Reported by Cary Valley and Michal Poborsky)
• Fixed an regression where features in replaced regions were erronously retained during restriction cloning if the insert was the same size.
  (Reported by Martha and James Smart)
• Fixed an issue with decoding features from GenBank files generated by CHOPCHOP.
  (Reported by Reuben Philip)
• Fixed aligning sequences in a multi-sequence FASTA file with a reference.
  (Reported by Fang Suo, Louise La Barbera Kastberg, Guttorm Haraldsen, and Ryan McNulty )
• Fixed an issue with opening supported file types in Miscellaneous Files when viewing a collection.
  (Reported by Dinesh Babu Paudel)
• Fixed a default file name and extension when saving a sequence trace.
  (Reported by Dinesh Babu Paude)
• Addressed an issue where Sharepoint index conflict files resulted in new file notifications when working with collections.
  (Reported by Andras Solt)
• Improved stability when detecting common features.
• Fixed an issue where the selection bar was blank after making a feature in a multiple sequence alignment.
• Fixed a crash when attempting to create a custom feature type in SnapGene Viewer.
• Fixed an issue that prevented loading non-installed custom feature types that are embedded within a file.
• Improved stability with multiple sequence alignments.
• Fixed a memory leak when creating, editing, or duplicating features.
• Corrected an issue with history colors after performing PCR using primers that extend beyond the end of a linear template.
• Fixed an issue with making RNA sequences from selections in large genomic sequences.
• Fixed an issue where unnecessary menus were sometimes shown on the launch dialog.
• Fixed various issues where characters right of a period in a agarose gel sequence name was not shown in the fragment list or source control
• Removed unecessary message indicating upgrading to SnapGene is required to perform an alignemnt if one or more aligned sequences and an associated alignment to the reference sequence is already computed.
• Improved overall stability
• Addressed various memory leaks.