SnapGene Version 4.1.4
SnapGene 4.1.4 was released on January 09, 2018.
Enhancements
- Enabled choice of a destination subfolder when importing into a collection.
- Enhanced the recognition of feature names when opening ApE files.
- Updated the common features database.
- Made various color enhancements.
Fixes
- Fixed an issue where sequences that align around the numerical origin were sometimes shown on top of other aligned sequences in linear maps.
(Reported by Leonid) - Prevented duplication of files when moving between folders in a collection on Windows.
(Reported by John) - Restored the ability to browse to a collection on Windows when using "Save to Collection".
(Reported by Carles Alvarez) - Allowed non-native files to be saved to the appropriate collection folder.
(Reported by Carles Alvarez) - Fixed a crash that could occur when opening the Preferences dialog on Ubuntu Linux.
(Reported by Olivier Bertini) - Improved the importer for DNA Strider files.
(Reported by Francesca Mattiroli) - Ensured consistent computation of the primer overlap length and Tm for NEB HiFi assembly.
(Reported by Nan Liang) - Improved map labels when importing certain protein sequences from NCBI by ignoring the KEYWORDS field.
- Removed the "Order" button from various dialogs where it was not appropriate.
- Prevented the "Order" button from being visible when no or multiple DNA sequences are selected in a collection.
- Ensured that aligned sequences that wrap around the numerical origin are always visible when viewing a downstream aligned region in Sequence view.
- Enabled unsaved sequences imported from NCBI to be saved to a collection.
- Allowed for simple case changes when renaming a file in a collection.
- Improved the behavior for dragging and dropping files in a collection.
- Fixed various issues with saving to a collection where the expected default folder was not always selected or the Save button was not always enabled when appropriate.
- Corrected errors with the rendering of site features in protein sequences.