leasebas.blogg.se - Snapgene viewer free

Snapgene viewer free for free#

SnapGene is so easy to use that my lab adopted it instantly.

Snapgene viewer free for free#

SnapGene Viewer SnapGene Viewer lets you see your data for free with the same rich visualization, annotation, and sharing capabilities as the fully enabled SnapGene software. Improved application stability when importing primers.Improved application tability when searching a collection for a named feature.Improved application stability when mousing over features.Improved application stability when hovering over aligned sequences.Improved application stability when quitting.Ensured correct scrolling of Sequence, Features, and Primers views in response to a change in the selection, but only when appropriate.Ensured that the Next button is the default control after searching a sequence trace.Prevented repetitive alignment to a reference sequence when making simple edits such as insertions, deletions, and same-size replacements.Restored import of ssRNA sequences as double-stranded rather than single-stranded DNA.Ensured highlighting of the inserted region for Gateway BP cloning in the Insert tab, and of the ancestral insert in History view for the resulting product file.Improved performance when showing the Add Primer dialog and other dialogs that provide controls for choosing files.Improved application stability when using the 'Find similar DNA sequences' command.Restored highlighting of the called base under the mouse when viewing sequence traces.Streamlined the side toolbar in the Insert Codons, Choose Alternative Codons, Browse Common Features and Insert Feature dialogs.Ensured that the enzyme set indicator does not occlude content after scrolling to the bottom of Sequence view.Corrected a misleading message that was shown when a problem occurred during program activation.

Improved application stability when searching for enzymes, features, and primers.

Enabled simulation of Gateway BP and LR recombination around the numerical origin.

Fixed an issue that could result in editing-induced disappearance of a sequence aligned to a reference DNA sequence.

Corrected a regression to restore transfer of primers when pasting a copied DNA sequence.

Improved the detection of sequence type when importing DNASTAR SeqBuilder files.

Populate the 'Description' fields when pasting GenBank content into the New File dialogs.

Corrected a regression to ensure detection of restriction sites whose recognition sequences span the numerical origin.

Improved application stability when dragging out selections.

Added DNA ladders from GeneBio Systems.