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.
#N gene sequence snapgene viewer series
Overall, SnapGene Viewer just as SnapGene, it's aimed more towards academic research and while the tools come with complex terminology and features, the viewer is a bit more accessible for viewing different DNA maps or sequences.Ī time series and frequency spectrum analyzer for engineers and scientistsVersion 5.2.4: New functionality: While the application itself has just a couple of features compared to its main SnapGene application, it's useful however for collaboration purposes or just to view different sequences quickly and with ease. The viewer allows anyone to see created DNA maps and works with big files, with a limit of 1Gb per file.Īn excellent feature of SnapGene Viewer is the ability to export a DNA sequence from the given map and save it as a GenBank format for further use and analysis.
#N gene sequence snapgene viewer software
It works very well in conjunction with Snapgene, a software that lets you create and edit DNA sequences and maps. No review No Video A user-friendly software solution that can come in handy for previewing your created DNA maps SnapGene Viewer is an excellent tool for viewing DNA maps with ease. To adjust the criteria for showing ORFs, specify the minimum ORF length and the start codon options, then click OK.
To open the Translation Options dialog, click View → Translation Options. User Guides SnapGene Translations Display Open Reading Frames. Visualize Create a DNA sequence file by either entering a sequence, or importing a record from GenBank, or opening an annotated sequence stored in one of many common file formats. SnapGene Viewer is revolutionary software that allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1 Gb in length.
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