![]() But Applications is the most convenient place to put things, so we suggest you just put everything there.ĭMG files are mounted by your system, like a sort of virtual hard drive. Some people create a “Games” directory, to keep games separate from other applications. You don’t have to put your programs in the Applications folder, though: they’ll run from anywhere. Then you can feel free to delete the original DMG file: you don’t need it anymore.When you’re done installing: just click the “Eject” arrow.And you’re done: the SnapGene Viewer is now installed.Simply drag the application’s icon to your Applications folder.Often these will include the application itself, some form of arrow, and a shortcut to the Applications folder.Double-click the DMG file to open it, and you’ll see a Finder window.dmg installation file from the official link on above Like if you wanna download SnapGene Viewer for mac from this page, you’ll directly get the. Most Mac OS applications downloaded from outside the App Store come inside a DMG file. Fixed an issue that incorrectly suggested a sequence trace has unsaved edits after using File → Save As.Fixed an issue that prevented looking up an enzyme by right-clicking in the Enzyme or Sites column in Enzymes view.Improved the toggling of enzyme visibility when repeatedly clicking check boxes in Enzymes view.Reduced the file size when exporting maps and history as PNG images.Ensured that bold is correctly used to highlight unique cutters after undoing sequence edits.Ensured that the chosen enzyme set and enzyme visibility are retained when undoing sequence edits.Corrected a regression that prevented imported primers from being restricted to those that have a unique binding site.Ensured remembering of a preference for showing additional binding sites that do not match at the 3′ end.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.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.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.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |