Added a "Copy Rich Text" command for selections in alignments, to provide the option
of copying either simple sequences or sequences with metadata. (Inspired by Leigh Harty and Nelson Ramirez)
Added Invitrogen's "pScreen-iT LacZ-Dest" to the list of Gateway® Destination vectors. (Requested by Aysegul Gungor)
Modified the statistics in pairwise alignments to show two digits after the decimal point
instead of one. (Requested by Robin Luo)
Added time estimates to various progress dialogs.
Improved the order of "Copy" actions in the Edit menu.
Made various textual, alignment, and spacing improvements.
Enabled export of a map or history while viewing any tab.
Ensured reliable import of primers copied to the clipboard using Microsoft Office. (Reported by Daryl Beckford)
Added support for dragging and dropping FASTA archives into the Assemble Contigs dialog. (Reported by Thomas Reinard)
Preserved zoom and split view display options when switching between files
in a collection. (Requested by Joon Park)
Enhanced the Gene Construction Kit importer to capture the full set of notes in the
"General Info" section. (Reported by Steve Stippec)
Improved stability when computing and viewing multiple sequence alignments. (Reported by Leigh Harty)
Corrected an issue that could cause features to be erroneously detected around the numerical
origin of a linear sequence.
Ensured that proper file extensions were included when batch converting files from one
format to another.
Ensured correct setting of the default button in the Find controls when pressing and
releasing Shift in a sequence trace window.
Corrected a regression with the navigation buttons when viewing an alignment to a
Addressed issues with the purple bar and the Tm column when importing primers from
Corrected the displayed molecular weight when adding a translated feature to the common
Removed the colors button in cloning dialogs, and streamlined the side toolbar in the
Edit DNA Ends, Browse Common Features, and Mutageneis dialogs.
Improved the display of long sequence names within circular maps.
Corrected a regression by removing cut locations for ancestral restriction sites in
Removed the inappropriate "Preserve feature annotations" control from the New File
dialog, and the inappropriate "Detect common features" control when inserting or
replacing bases in a sequence trace window.
Improved stability when assembling contigs using FASTQ data.
Disabled the Show/Hide All Enzymes commands when viewing protein files.
Corrected an issue in which the endpoints of a selection were not updated in the selection
bar after renumbering the origin of a linear sequence.
Fixed an issue that prevented immediately using SnapGene without restarting after
activating a Flexera-based shared license.
Corrected an issue with computing % GC when partially degenerate residues (B, D, H, and V) were present.
Ensured that only the zoomed region is shown for the root map in History view.
Addressed an issue in which the Save As dialog would vanish immediately when attempting
to choose a different name instead of saving over an existing file.
Ensured that enzyme set menus are refreshed after using Manage Enzyme Sets.
Ensured that the desired endpoint modifications are correctly applied when designing a
Improved the registration of file associations on macOS.