Corrected an issue that prevented saving a new file created from a selection from being saved to an open collection.
Corrected an issue that could cause pop-up menus to remain open when the Launch dialog was closed.
Improved the message shown if an alignment is selected in a collection.
Improved fonts and text placement in History view.
#Snapgene viewer version windows#
Addressed issues that prevented collections stored on Windows network shares from being listed as recent collections in the File → Open Collection menu.
Ensured correct export of common features to the specified folder.
Corrected various issues that could occur when attempting to add features to the common features database, or importing such features, if they were marked as not visible in the original document.
Corrected an issue that allowed duplicate primers with the same name but different sequence case to be imported into a file.
Ensured correct enabling and disabling of the “Edit History” control in History view when the history is modified.
Fixed an issue in which the text representation of History view did not always refresh immediately when edits were made or undone.
Addressed an issue with importing some Vector NTI Express databases.
Fixed an issue that prevented importing from Vector NTI databases on Windows.
#Snapgene viewer version manual#
Improved manual adjustment of vertical scaling of sequences traces aligned to a reference sequence.
Removed the “Hybridization Parameters” menu action when viewing an RNA sequence in a collection.
Fixed an issue that could cause custom common features to be corrupted by using the right-click context menu to edit a common feature.
Improved button placement in History view.
Made significant stability improvements.
Enabled “File → Export → Alignment…” and “File → Export → Consensus…” when viewing an alignment.
Completely removed the installation folder when uninstalling on Windows.
Prevented a crash that would occur after double-clicking when importing SnapGene and Addgene online sequences.
Prohibited pasting when multiple files are selected in a collection.
Allocated sufficient space to display the “Size” column in Features view when viewing ssDNA and ssRNA sequences.
Preserved the display of preferred codons when switching between DNA and mRNA formats when viewing a codon usage table.
Fixed an issue where File → Save did not work after redoing an unsaved alignment.
Ensured retention of unchanged alignment name and omission of name controls when using the “Replace” option when redoing an alignment.
SnapGene Viewer is a versatile tool for creating and sharing richly annotated sequence files.